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

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EnhancerAtlas ID
HS105-52814 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr22:29913360-29914450 
Target genes
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CREB1MA0018.3chr22:29913373-29913385GATGACGTCACA+6.02
CREB1MA0018.3chr22:29913373-29913385GATGACGTCACA-6.02
ESR1MA0112.3chr22:29913521-29913538CATGTCAACCTGACCTT+6.17
JDP2(var.2)MA0656.1chr22:29913373-29913385GATGACGTCACA+6.32
MIXL1MA0662.1chr22:29913671-29913681GTTAATTAGA-6.02
Nr2f6(var.2)MA0728.1chr22:29914240-29914255TGAACTCCTGACCTC-6.22
RORAMA0071.1chr22:29913713-29913723TGACCTTGAT-6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr222991348929913826
Number: 2             
IDChromosomeStartEnd
GH22I029517chr222991366129913690
GH22I029518chr222991370129913810
Enhancer Sequence
AGAGAACAAG ACAGATGACG TCACAGGTAG AAATCAGGTG CCACAGATGG GTAACTAGCA 60
TCCTCCTGGG GCTCTCTGAA GGGCTCAGAT GGCCCGGCCA GCTATCCTGG TATACCTGGT 120
ACTCAGGAAG TACCCAGGTC AACACGTGCC AGGAATGCAA GCATGTCAAC CTGACCTTCA 180
CCCAGTGCTA TGTGCTTGTG GCCAGATCCA GTGCCAGCAC TTATGGTGCT TTCTCTTTAA 240
TGCAAATGAT AGCCTGCCAA AGAAAAACCC TTACAGTCAG AACTAGGGAG GGTGCCCCTG 300
CAGCAGTGAC TGTTAATTAG ATCAAATAGC ATAGAGGCCT GTGTTTTCAT AGCTGACCTT 360
GATGGAGGAA ACAACTGAAG TGTTGTGTGT CAGGGAGAAG AGCCAGATAA CTGCTCCAGG 420
GTAAATTCCT GCTGGCATTT AAATAAGCAA ATATGCCAAC ACAGTAAGTA CTGTCCAGAA 480
TGACAAGTTC CCTACCTTGG GACAAAACAA ACTCAGCAGT GCTGATGGGG AGCACGGCCC 540
GATGGACAAA CATCAGTGCT CTGGAGAGAT CGGCAGCCAT GTGGAGTCTA AGAACTGGTG 600
GGGAGTGGTC TCCAGATGTG TCCTGGAAAC CCAATGCCTT TCCTGACAGA GACTCTTTTT 660
TATTTTTTAC TTTTTATTTT GAGATGGAGT CTCGCTTTGT TGCCCAGGCT GGAATACAGT 720
GATGCGATCT CAGCTCACTG CAACTTCCGC CTCTCAGGTT CAAGCAATTC TCCTGCTTCA 780
GCCTCCTGAG TAGCTGGGAA TACAAGTGCA CACCACCATG CCCAGCTAAT TTTTGTATTT 840
TTAGTAGAGA CGGAGTTTCA CCATGTTGGC AGGCTGGTCT TGAACTCCTG ACCTCAAGTG 900
ATCTGTCTGC CTTGGCCTCC CAAAGTGCTG TGATTACAGG CAAGAGCCAC TGCGCCTGTC 960
CCAGAGACTC TTTTAGGTCA GAAAAATCTT GACCCCATCC CCCTGCCACA TGGTAAGCAT 1020
TTGACAACCA CTTACTGAGT GAATAAACTA AAAGAAGCCC CCAAATGCCA CCACCTAAGT 1080
CAGTGGCTCA 1090