Tag | Content |
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EnhancerAtlas ID | HS044-11208 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr6:29520280-29521770 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYA | MA0060.3 | chr6:29520543-29520554 | TCTGATTGGTT | - | 6.62 | NFYB | MA0502.1 | chr6:29520544-29520559 | CTGATTGGTTGAGCT | - | 6.31 |
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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: 2 | ID | Chromosome | Start | End |
GH06I029552 | chr6 | 29520395 | 29520654 | GH06I029553 | chr6 | 29520978 | 29521937 |
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Enhancer Sequence | AGTAATCAGC CGTATAATGG GTTGTGTTAG AAAGTAAACT AAGGCCCAAT AAAATATTTA 60 AGAGTTTATT TGAGCAGTGA TCCAGAAGTG GCTAGGGAGC TCCCCAGAGA GAACATGAGG 120 AGGAGGCTTT TTAGGACAAA TAGATAAAAG CAAAGATAAT ATTTCATTGG TTACAGTTAT 180 ACAGTTACAC AGTTATACAG TTGCCTTATT TGGTCTATCC CATGAGGAAG TCCTAGTTAC 240 TAATTACGTT TTTGTTGGCT GCTTCTGATT GGTTGAGCTT AAGTTCTGTG TTTCTTTAAC 300 ATAGGCATTT ACAAGAAATA CCACAAATAA AGTTTCAGAC ATGCTTGCAA ATCAAGCAAG 360 GTTAAGGTCA CTTAGGAGGC CCAACTGGCT CTGTCTGCTC AAGGATTCTT CTGGCCTCGT 420 CTCCATTTTA CATGAACTGT TGCATAAATA AACACAGAGT ACCTGAAACA ACGGAGGTGA 480 TCATTCTGCC TACCGAGTGT TGGCCAGGCC AAGCTTGGAG TGTTGCTCTT ATTCTTAGGG 540 AGTTTATTTT TAAGTAATCT CATCTGTAAA TGGGATTACA ATCCACAAAC TGACCTTGTA 600 TATGATTCCA TTCCTTCTCC CAGCCCAGCC CCACACTCCA AGGTTTTCCC TTTGCTTATA 660 AGGGGTAGTC ACCCTTTTTT ATTTCGACCT TCCAAACATT CTGGGAGTTT TCCTCCTTTA 720 GGCCAACTAC AGCGCAGAGG AGCGCTTTCT CCTGCTGGGT TTCTCCGACT GGCCTTCCCT 780 GCAGCCGGTC CTCTTCGCCC TTGTCCTCCT GTGCTACCTC CTGACCTTGA CGGGCAACTC 840 GGCGCTGGTG CTGCTGGCGG TGCGCGACCC GCGCCTGCAC ACGCCCATGT ACTACTTCCT 900 CTGCCACCTG GCCTTGGTAG ACGCGGGCTT CACTACTAGC GTGGTGCCGC CGCTGCTGGC 960 CAACCTGCGC GGACCAGCGC TCTGGCTGCC GCGCAGCCAC TGCACGGCCC AGCTGTGCGC 1020 ATCGCTGGCT CTGGGTTCCG CCGAATGCGT CCTCCTGGCG GTGATGGCTC TGGACCGCGC 1080 GGCCGCAGTG TGCCGCCCGC TGCGCTATGC GGGGCTCGTC TCCCCGCGCC TATGTCGCAC 1140 GCTGGCCAGC GCCTCCTGGC TAAGCGGCCT CACCAACTCG GTTGCGCAAA CCGCGCTCCT 1200 GGCTGAGCGG CCGCTGTGCG CGCCCCGCCT GCTGGACCAC TTCATCTGTG AGCTGCCGGC 1260 GTTGCTCAAG CTGGCCTGCG GAGGCGACGG AGACACTACC GAGAACCAGA TGTTCGCCGC 1320 CCGCGTGGTC ATCCTGCTGC TGCCGTTTGC CGTCATCCTG GCCTCCTACG GTGCCGTGGC 1380 CCGAGCTGTC TGTTGCATGC GGTTCAGCGG AGGCCGGAGG AGGGCGGTGG GCACGTGTGG 1440 GTCCCACCTG ACAGCCGTCT GCCTGTTCTA CGGCTCGGCC ATCTACACCT 1490
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