Tag | Content |
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EnhancerAtlas ID | HS092-29797 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr4:2747610-2748840 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr4:2747655-2747673 | GCAGGGAAGGCAGGAAGC | + | 6.28 | FOSL2 | MA0478.1 | chr4:2748036-2748047 | GGGTGACTCAG | + | 6.02 | JUNB | MA0490.1 | chr4:2748036-2748047 | GGGTGACTCAG | + | 6.02 | RREB1 | MA0073.1 | chr4:2747866-2747886 | CCACAACCCAAACCAACCCC | + | 6.29 | RREB1 | MA0073.1 | chr4:2747871-2747891 | ACCCAAACCAACCCCCACTA | + | 7.36 | TFAP2A | MA0003.3 | chr4:2748121-2748132 | CGCCTCAGGCT | + | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_53166 | chr4:2747023-2748909 | Small_Intestine |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I002745 | chr4 | 2746834 | 2750071 |
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Enhancer Sequence | TGATAAAGTC TTCTCATTGC CAGAGATTTG CCATTATCAC AGACAGCAGG GAAGGCAGGA 60 AGCTGAATCC CATTGTAAAC CAGAGGATCT CCAGTGAGGG GGCCCCCAGC TGCCCAGGGT 120 GGGCCTGGCC ATGCACCCTG CTTACCTCCT TTGGAGCCCA TGACACTGTC CTGTCTGCAG 180 ACAATCGGGT TCAACCAGGT GATTCTGGAC ACAGGAATCT AACCTCTGCC CCACGCAGGG 240 TCAGGAGTCA CCGAAGCCAC AACCCAAACC AACCCCCACT AACAACTACA GAGCTGAATG 300 AAAAGTCTCC TGAAACTCGT GTGTACCCTA CAATTCTGAC TGTATCTCAG TGACATAATT 360 TTTGAGAATT CCCCTCAAAT GACAAAGGAA GTGCACGTCC TAACACAGCC TACACCGGGA 420 AGCCCCGGGT GACTCAGCTG AGTTCAGGGC TGAGAAGTGA CACTTATTTA GAGACTGTGA 480 TGAGGGCCTA CCCTGCCACT GGCCCCACCC CCGCCTCAGG CTCAACACTG TGTGTGGCTC 540 CTTTCAAATC CCCAGAGGGA AATGACACAG TGACTCAAAA TCAGACCAGA ACACCCTGCC 600 TCCGCCCAGA CGGCACTTTT CCTCTGGTTT CTGAATGCAG CTGTGTCCTC TCTGAGGTTC 660 CCCGCCTGGA ATCCACCCAG CTGAGGTGGG CAGTTCTCAG ACCAACCTTC TCCCCAGTGG 720 GCGCCTCGGT GAAGCTGCTG ATGGGTGCGG GATGTACTGT CTGCCACAGA ACATCCCAGC 780 GCGTGTGTTT CTGCATGAAC CTTGGTGCTG CCTCAGAGAA CTGCCTAGAA AGGACCCGAG 840 CGAGAGGCCC TGTGCCCGGC AGTGCGAGTG AGATGGGGTC TCAGCCTAGG TGAGATGTGC 900 ACGGAGTGCC TCCATTCCCC TGCCTGCCAC ACACAGACCA CCACAAGCAC CAGCAAGATG 960 GAAGGTGCCT GGCACACAGA TGCCTTGGGC CACTGCTCCC CTACTTTTCT GCCTAGGAGC 1020 CCCCTGGTTT CTCCTGATGC TGAAACTCCC ACGGTCCTTC TCTCTCCCAC TAGACCCCAC 1080 AGAGAGCTAC AGCCCAGATC CAGCCTATCC TGGAGGTCCA GCGAACCCTT CTTTGGCCCT 1140 CACTGTCACT TGGTGCCGCT GCCCCCGGCC CTTGCTTTGA TGATGAGGAG GCTGTGGCCC 1200 TGAGCCAGGT CTCCAAGCTT GCGGGAGGCC 1230
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