Tag | Content |
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EnhancerAtlas ID | HS194-05106 |
Organism | Homo sapiens |
Tissue/cell | Urothelial_cell |
Coordinate | chr7:2081020-2083280 |
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) |
NRF1 | MA0506.1 | chr7:2081865-2081876 | GCGCATGCGCA | + | 6.32 |
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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 |
GH07I002041 | chr7 | 2081068 | 2081519 |
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Enhancer Sequence | GCAGGAGCCC ATCCCTGCCA GCCCCAACCT GCCAGCTCGT AGCAGAGTCA GCTCATCACA 60 TTCATGCTAC CCAACCCTCT TGCTGCTTTC TGTAATTTTT CACTTCCCTG ACTCCATTTG 120 GGCACCTGTT CCCCACACTC CCTTTAAAAT GCCCAGTCAC ATCTGCACAA ACCTGAAAGG 180 AGCTCAGCTC TGTCCCCTGC TGTCAGCAGC GACTGAATAA AATCTGTTTT CTCCACTTTA 240 ACTTACATCC AGCTGCATAT ACCTTTGACA TGGGTCACGA CTGACGCTTG ACATGAGTTG 300 AATGAAACCA GATGAGGAAG AGCTTTGAAG GCATACCATC AGGTGTCAGG TCACTAACCC 360 TCTCTTTGCC CGAGAGGAGT AGAAAACTCC ACAAGACAGT CTCACTTCCA CGCTGCAAAA 420 ATGTCAACTC TCACCATGGC AGCCCACAGG GGGGAGGGAT ACTGAACACA AAACTCACTC 480 AGGTGCCTGC TTTGGCCTGG CCACGCTGCA CCCAGCTCCC CGCAGCACCT CCTGCTCTGT 540 TCCAGAGAGG CGAGCAGAGC CTGCATCCTA CCCAGCCAAG GCCAGAGAGA ACTAGCTCCC 600 TGGGAAAGCA GCAAGGGACC ATCCAAGAAA GACTTAGACA CACACACGCA CACGGACATG 660 CACACAGACA CACAGATGCA CGTACACACA TATGTACACA CACATCCACA CACGCACATG 720 TGCACACACA CACGCAGACA CACATGCACA CGGACATGCA GACATGCACA CACATATGTA 780 CACACATACA CATGCACACA CACACGCACA TGGACACAGA CACGCACACA GACGTGCACA 840 CACAAGCGCA TGCGCACACG TACACAGACA CACATACGCA CATGCACACA CACGCGCACA 900 TGGACACAGA CACACGCAGA TGTGCACAGA CACACAGGCA CACGGACACA CGCACAGACA 960 CACACATGGG CACACAGGCA CAAGGGCATG CACACGGCAT TCCTAACTGC CACCACCGAC 1020 CTTTTCACAC TCCAGCCACC CCAGAACCCT GGCGTTTAGA ATCTGCAGCT AAAATACACC 1080 CAATGATGGT ATCAACGTTC ATTTATTCAT TCAACAAATA CTTGGCGATA TGGTTTGGAT 1140 GTCTGCTCCC TCCAAATCTC AGGTTGAAAA ATGTTTCCCA AAGGTGGAGG TGGGGCCTGG 1200 TGGGAGGTGT TGGATTATGA GGGCGGATCC CTCACGAATG GCCCAGAGCC ATCCCGAGTG 1260 AGGAGTGTTG TTGGAAAGAT TCTGGAACCT CAAGTGTCTC TCTTGCTCCT GCTCTTGCCA 1320 TGTGACGTGC CTGCTCCTTG CCTTCTGCCA TGATCAGAAG CTTCCTGGTA CCTCAGCAGA 1380 AGCAGATGCC GGCGCTGTGC TTCCTGTACA GTCCGCAGAA TGACCCAGCC TCAGGGATTC 1440 CTTTATAGAG ACACAAGAAC GGACTAATAC ACCTGAGGAG CCTTCACGCA CACACATGTC 1500 CACGTCCACG TCCACGTCCA CATCCACGTC CACGTCCACA TCAAGGCAGT GCTGCTGAGG 1560 GCCAGAGGAC GCTGCCACAG GCCGACCCCG TGAAGCTGAA AGTCACCTTC GCCAAGAAGG 1620 ATGGGCTTCT GGAAAACACA GCCCTGCACT TAGAAACTTC AGACCCTACT CTCCACAATC 1680 TCTTTATTTA TAAAATTGCT TATGCGAAGA TATTTCCACG CAGAATGCAT TCAATTATGC 1740 AGTGTAAGGG GGGGCCTGAA TGGAGAACAT CCAAGTCAGC CACGAAGACA CTTCAGGAAA 1800 TACAAGAAAA CGACCCTGCC ACTGACTTTC GAATGTGTCT GCATCCACGC CCCTGTCCCA 1860 TCGGAGGGGC ACAGGGTAAT ACATAGCACT GCGCTCCCCT CCTTCTCCTG TGGTTCCCCT 1920 CCTGACAGCG CAGTGCAGTG CGGCAGACAC CCCTCATCCT CGGTGTCAGG GCAGCATTAG 1980 CATGTAAATA GCTGGCAGAC ACAAGGACGT GAAAGCAAGG AAGAGCTCTT TAATTAACTT 2040 TAATCCTCCA AAAATCCATG CTGCAATCTG TTCTGACAAT CCCACGCTCC TTAGGAGGCC 2100 CTCGGCACGA CCTGGCACAT CCTGTGGGCT GGAGGTGGCC GGAATGGGCG GGCTTGGGAA 2160 CGTGATGCCC GGGTACCGTG CCTACAAGGA CGCTGGGTCA TGACTGTTCT CTGGAGGCTA 2220 CGGGTGCCCT GCAGAGTGGA GGCACGCGGA GGGCCTGGGG 2260
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