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

TagContent
EnhancerAtlas ID
HS002-06307 
Organism
Homo sapiens 
Tissue/cell
A375 
Coordinate
chr21:34754690-34755920 
Target genes
Number: 4             
NameEnsembl ID
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
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
chr213475470834755048
Number: 1             
IDChromosomeStartEnd
GH21I033378chr213475110834757769
Enhancer Sequence
CAGAGAGGCC CAGTCGCTCT TCTCAGAGTC TCCGTGGCAT CTCGGTAGAT TTGCTGATCC 60
CTTTACATAA CCCAAGTTGA GGCATGCCCT AATTTCACCC ACAAATGCTA CTAAGCCCAG 120
GCCCTTATCC AGCCAAAACC ATCCTGCCAA GCTCCCACCA CCACCATCAG CATCATTTTC 180
AGGTTGTTGG TCATCACTGG TTGTTGGTCA TCACTGGTTG TTGGTCATCT ATGTCACCTA 240
ACAGGCCACT CATGACGTTA GCCCTTGACT TCAAAAAGGA CCTCAAAGAA AATTCCAGTT 300
TTCACTCCAA AAGGAGAAAT CAGGCCGAGC TGTGATGGCT CATGCCTGTA TTCCCAGCAC 360
TATGGGAGGC TGAGGCAGGC GGATCGCTTG AGCCCAGGAG TTTGAGACCA CCCTGGGCAA 420
ACCTATCTTT CCAAAAAAAT ACAAAAAGAT TAGCTGGGCA TGGTGGTGCG TGCCTGTAGT 480
CTCAGCTAGT CAGGAGGCTG AGGTGGGAGG ATCACTTAAG CCTGGAAGGT TGAGGCTGCA 540
GTGAGCGGTG ATGGTGCCAC TGCACTCCAG CCTGGATAAC AGAGCAAGAT GCTGTCTCAA 600
AAACTAGCAA ACGAAACAAA AGGAGAAACT GCTGGCAGCC CCTAATCTAG TACTGTCCCG 660
GCTCCACCCA CCTTCAGATC CAGCCTCCTC CCCTGGCACA CGGGAGCCCC CTCCTCTGAC 720
TGTGCTGAAA GTGAGGGAAG ATCCCCTCTG GGGAGAGAGC TGTAGCCTTG ACCTCTGCAC 780
ACCTTACTTA TCCAGAGCAC GAGGCAGGGC CGCTGACTCA TCCTGGTTTA CCCTGGGCTT 840
TCCCAGTTTC AGCACTGAAA GTCCCGCATC TGGAAAAGCC CCTGAGTCGC TGACAAACCA 900
GACAGTCCGG ACCATGCAAA GCACAGTGCA TGGTGCTTTA GCCACAAAGT TGATTGAAAA 960
GTCAGAGGCA GTGAGCCACA GGAAGCGCCA CGTGACCCAG ACTGCGAGGA GGACACAGGA 1020
AACCAACCCT CACTGTGTCC TGCTAGGGGG TTAACCCGTC TACAAGCATC AGGGTTGCCA 1080
TTTCAGAGAT CAGCAAACTG AACAGCAGTC GTGACTTGTC CTCGCCTGCA AGACAAGCGA 1140
GTAACAAATC CATGAAGGGA AGGACACGGA ATTGAGCAAG GGGGCAGGGC CGGATGTCAT 1200
TTTGGCGTTT TTTTTTCTTT CAGTGATTGA 1230