Tag | Content |
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EnhancerAtlas ID | HS092-15059 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr13:98891270-98892690 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr13:98892631-98892649 | GGCAGGAAGGGAGGATGC | + | 6.12 | Nr5a2 | MA0505.1 | chr13:98892548-98892563 | GCTGGCCTTGAAACT | - | 6.16 | ZNF263 | MA0528.1 | chr13:98892282-98892303 | GAAGGAGGCAGGAGGGGAGGT | + | 6.7 |
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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 |
GH13I098239 | chr13 | 98891737 | 98892467 |
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Enhancer Sequence | GTCTGATTAG TGGTATGGAT GGGGTCTTAC CTGTTAAAAC TCACAGGGAA TTGGACTTCC 60 TTATGGGTTA ATGTATCTAC AGACTACTTT CAGCATATTT TTGAAGATTT ACTGCAGTTG 120 TGGGGAAATA ACACCAGCAT TCAGTATATT GAACACTTAA GATACTTACC CTATGGAGAA 180 AGGAGCCCCA AGGGAACAAG TGCCGGTTTA CGCAGCTGTC TCCTATTAGG TTCTCTACCC 240 TGGACCGACC CTGGTTGTGT TTTCTCTCCC TCATCCCATC ATAAAAACTG GAGCCCACAT 300 CCAGGTTCAG CCAAGGCCCT CAGGGCAAAC ACTGGCTCCA CTGCCCCTTT ATTGCGTGCT 360 TGCAATTGGA GCTCTTTGGG CCTGAGTTTC CTTACTGTTT TGCTTGATCA GCAGTGCGTT 420 GACAAAGATG TTGTTTATAT TTTATCCAGC ATTTTTAGCT GTTTCATACG ATTTCTACAC 480 TGTGGAATCA TTTTAAGTGG TGTGAGGGGT GGAGGGGGAG GAGACATGGC TGGAGCTGAA 540 GAACTGATCT CCAGCATGAG TGGGGCTGAG GTCCGGATTA GGCAGTGCTG TTAGAGACTC 600 CAGCAGGCCT CAGGCAGGGA TGGCAGGCAC CAAGTGGCCT GGGGGCAGTG GGGAGAGGTG 660 GTCCCTTGGG TTTCTGGCTG GGCCACTGAG TGGCGGGTGG CATTGGTTAT TGAAGGGCTG 720 CTCCCGGAGG AGATGAGCGG GGAGGGGGTG CTCAGGTGAG ACTTCTGGGG AGCAGGTGAC 780 TCTCTGGCTC CAAGCGGGGA GCCCCACCTG GACTTGCTGG TGGGGCTGCT GGTCCAGACT 840 GTGCTAGAGG AGAGAGAAAG GGCTGCTATT GTTTGCCTCC CAGCAGGTGA AGGAGGAGGG 900 GCCCAAAGAC ACCTGGGCAG GTAACTTCAT CAGGAAGACG GCTACCTCTC TTCTCCAGAG 960 AGCGAGAGTG AAGTGAGCAG GTGATATCCG TGGTGATCCC TCCACAAGGA GGGAAGGAGG 1020 CAGGAGGGGA GGTGGCTTTA GCTCCCTTTC CTTTAGCCCT GTGGACTGGA GGGGCCTTGA 1080 TCATCTCTTC TACCCTTGCA CGGGGTCACC CTTGGCCAGG GACGCCTGTG GCCAGTGGCT 1140 GGGGCCTTGT GCTGCTTAAA GCATGAGTTA TTAGCACAAC CGATTCAGGG TAGACGCACG 1200 TTTTTTGGGA CTTTTGGAAA AGGAACACGC GATGACGAAT GAATGATTAG ATCTGAGGCC 1260 TTGGAGGGGT CAGCGAGTGC TGGCCTTGAA ACTCAAGCTG CTTTGGCCTT GGTGGGAGTC 1320 TTGCCTGCGT GGTGATGGTG ACGGTTGGAG TGGCCTTCCC AGGCAGGAAG GGAGGATGCG 1380 GCGATGCTCC CAGTTTATTG AAACCTGACT TTGTTCCCTG 1420
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