Tag | Content |
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EnhancerAtlas ID | HS044-10557 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr5:106841590-106842340 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr5:106842028-106842043 | AGTAAATGATTAACC | - | 6.49 | HNF1A | MA0046.2 | chr5:106842028-106842043 | AGTAAATGATTAACC | + | 6.9 | HNF1B | MA0153.2 | chr5:106842029-106842042 | GTAAATGATTAAC | - | 6.39 | HNF1B | MA0153.2 | chr5:106842029-106842042 | GTAAATGATTAAC | + | 6.87 | NFAT5 | MA0606.1 | chr5:106841593-106841603 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr5:106841593-106841603 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr5:106841593-106841603 | ATTTTCCATT | + | 6.02 | TFAP2A | MA0003.3 | chr5:106842299-106842310 | TGCCTGAGGCA | - | 6.02 |
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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 |
GH05I107505 | chr5 | 106841568 | 106842428 |
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Enhancer Sequence | CCCATTTTCC ATTTGAGAAA ACTGAAGCCT AACTGAAGTA GCTTGCCCAA GGTGATAGAG 60 CTAGTGAGCG ACAGAGCCAA GATTTAAACC CTGGCAGTCT GATCCAGTCT ACACATTCAA 120 CCACTATGCT ATATTGCTCT AAAGCACAAC CACAGGGAGC CACAAGAAAC ACTTCAAGCT 180 CTTGAGCACT TACGCTTTAT TTGTGTACCT CTCACTGCCT GAAATGACTC CCAGCTTAGG 240 ACTCACCAGC TCCATGAACC CTTCCCAGAT TTCCCTCAGG AACAGTTGTC TACTCCCTTC 300 TCTGGTCCAT CAAGATATCT TGTACATATT CCAAATTCTG TACTTATTGG AACTATATTA 360 TAACTATTTG TCTGCATGTT TGCTCTTTTT ATTCGTGAGG CTTGGCTGAG AATTCAACAC 420 ATAGTAAACA TCCAGTAGAG TAAATGATTA ACCTGTCATT GGAACATTAC AATTTAGTTG 480 AAGAAGTAGT CTGAACTCTA TTGGTGTAAG TATTTGTGTT TGATAATGGC AAATAAGAAT 540 AAAGGTTACC TTAGCAAAGG TTGCTAAATT ATGGACTGGG GTGAAGATAG GGCTCAAACC 600 TCACTCTGAT AGACCTTAAA GGATAGGAAT GAATCAGATG ACTGGAAAAG AGGAGAGGCA 660 ATCTGGGGCC AGATGAGCAG GAGCAGGAGC AGGGGATTTG AGAAATGAGT GCCTGAGGCA 720 GGTGTGGAGG GTGGGCAGCC CATTTAATGG 750
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