Tag | Content |
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EnhancerAtlas ID | HS044-10427 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr5:72673740-72674660 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr5:72674353-72674364 | GGGCGGGAAGA | + | 6.14 | MSC | MA0665.1 | chr5:72674048-72674058 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr5:72674048-72674058 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr5:72674048-72674058 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr5:72674048-72674058 | AACAGCTGTT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 72673992 | 72674146 | chr5 | 72674372 | 72674422 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I073378 | chr5 | 72674021 | 72674150 |
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Enhancer Sequence | TGATCTTTAC CATATCTGAA GCCCTCCCCA ACGTAAGAGG TCAAGGCTAG AACTTGCTAA 60 TAACCATCAG AAGCTGGAAA TTCTGGATCA AACATTTTCT CAAACAGAAA GAAGTATTTG 120 CTTCCAAACT CCAACCAGGT AACAATGGTC TAAAAAATGA CTAGAAATGC AGCCGGTGTT 180 TCACTGTGGT TATTCTTTCT AATCACATAC AACATTTCAA GTACTTTCCT TAAATCACTC 240 CCAGGCAGTG AAGTCCTTTA TATTCATCCT GTGATGGCGG CAGCCTTGTT GGGCAGTGTT 300 TGTCCTAAAA CAGCTGTTGA GATCCTAGCA GGGGATCCCA GCAGGGGAAA AAAGTCACAT 360 GATTCTTTAG CTCATAAACC AGCTAGTTTA TTTTCTCGAG GATACATTAG GTAATCATGC 420 TGATGCAAAT AGCAAAGCTA GTAGCCCGGG GTTAGTAGCC AGAAATGGAG CTCTCTCACC 480 TCACCTCTCT CATCTCACCT CATCTCTACT GCTGGTAGAG AATGATCCAG ACGATATATT 540 CAGCACACAC ACAGACCATG GGTTCCAGCT CTGCCCCTCA GTTATTTTCT GCTATCTACC 600 AACAGAGCAG AGAGGGCGGG AAGAAAGCAC AAAACTGAGC CTGGCCCCAT CTGGCTGCTG 660 GCTTCCCAGC TCCTCATCTG GTTTTCTCTC CCACGTGGCC TGAAGACCAC TTGCTTGGGT 720 GACCCAGAAA ATATTCCTGT GACCTGTGCC TTTCCCCATG CTCTAACCAT ACCGCCAACA 780 AGCCAGCGGC CTCCTCACTG CATCCTCTCA GCAATACTAT ATGGGCCCTT CCTACTATTC 840 TAAGTCTTCT CAGTCTTTTC TCCCCAAGTG AATTAGAGGC TCCTAAAGAG CAGGAAATCC 900 ATATGCCTTT CATTATTGCT 920
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