Tag | Content |
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EnhancerAtlas ID | HS044-00610 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr1:95268700-95269860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr1:95268888-95268908 | CTCCCCACCACCACCCCACA | + | 6.23 | RUNX1 | MA0002.2 | chr1:95269257-95269268 | GTCTGTGGTTT | + | 6.62 |
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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 |
GH01I094801 | chr1 | 95266548 | 95270865 |
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Enhancer Sequence | ATAAAATTTA GAATGAGAGA TAAAAGGAAA AAGAAAAGCA AAGCAAGGTT GAGGAGCAAA 60 TAAGAGGGAA GAGAACATCA GAGAGCAGAA ATGTGGCAGG AGCAGGAAGA GGCCCACACA 120 CAGTAAGACC CCGGGACAGA TTCGAGGCAG CAGACAGGGC TGGGGCATTC AGTGTGGGGC 180 AAATGGGCCT CCCCACCACC ACCCCACACA AATTGCTCAC AATAATCCTC AAAATTAGCA 240 CTTAGTACAA TCATTTTTGT TACTAATAAT GACTGTATGC CTTTGAGAAA GTTGAGGCAC 300 ACAGTTCCCC CACTTAAAGC AGCAATATTG ATCTATTTCA TTATAATGTT ATTTGTCTCT 360 TAAATCACTT GTTATAAAAG CAAATAGATA TATCAACCCA TAAAAGACAC AATGGTTTAC 420 ATTCTTCATG CTCTGAGTGC TGCTGTAAGC CCTGTGACAA CAGCTGTGCT TTTTGGCAGT 480 GAACATGAAC TCACATCTGT CAGTGCTGTC AGCCATGGAG CCCTCTCCTG TCCCATCCTG 540 AGCTGATATC CAGCACTGTC TGTGGTTTAC CCCACCATGG CCTTGTTGCT TGTAATTTAA 600 TTTGTGTCCT AGAAAACAAC TATGCCTGGA TCAGCCCTCT ACACATACAA GGTTTCTGTG 660 AAGGGAGCGC CCAGGGTCAT CCAGTCAAAT TGGATTAGGG CCTAACCTAA CAACTCTGTT 720 TTAACTTAGC TACGTCTTTA CAGGCCCCGT TTCCTTTTCT GCTTTCCCTC TCTCAGAACA 780 AAGACAGCAC TGTTGTGAGA CAGAGTAGGG ATGGGACTTG ACCTCCCTCC CCCATGCCCC 840 ACCAAGGACT TTTACTGCAA GCTGATCGGT CTGTGGGGAT CCCGATCAGA CCATCCAGAC 900 CTTGCATCAT AAATCTGAGG TATTAGGGGT TAGGGCTTCA ACATATGAAT TTGGGGGGAC 960 ACAATTCAGC CCATAACAAA TGTGAACTTT TAAAAAGTTA ACCTCAGTTA TCGAGAACTC 1020 TTGCTCACCA ATCTAGAATC TCATTTTCTG ACAGCCTCAC ACAATGGAGT TGGCACTTCT 1080 CTGGCATCGT TGTCATGCCA GACCCGTTCA TGACTGTGGC AGAAGCTCCT GCAAGTGCAA 1140 CAACTTGTGA AAGATGCACA 1160
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