Tag | Content |
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EnhancerAtlas ID | HS023-22770 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr7:7455110-7456570 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr7:7455652-7455667 | TGAACTCCTGACCTC | - | 6.22 | SPI1 | MA0080.4 | chr7:7456001-7456015 | AGAATGAGGAAGTA | + | 6.18 | SPIC | MA0687.1 | chr7:7456001-7456015 | AGAATGAGGAAGTA | + | 6.87 |
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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 |
GH07I007414 | chr7 | 7453790 | 7457050 |
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Enhancer Sequence | CCTGCTACCA ACTGGATGCC AGGCAATCCA ATATGTCTAA AGAGGTTTTT CTGGTTGTTT 60 TGTTTGTTTT TTGAGACAGA GTCTAACTCT GTTGCCCAGG CAGGAGTGCA GTGGTGCGAT 120 CTTGGCTCAC TGCAACCTCC GCCTCCAGGA TTCAAGCGAT TCTCCTGCCT CAGCCTCCTG 180 AGTAGCTGAG ATTACAGGTA CGCACCACCA TGCCTGGCTA ATTTTTGTAT TTTTAGTAGA 240 GATGGGGTTT CACCATATTG GTGAGGCTGG TCTCAAACTC CTGACCTCAT GATCCACCCA 300 CCTCGGCCTC CCAAAGTGCT GGGTAGTTTT CTTTTTTTGG GAAGACAAGG TCTCACTCTG 360 TCATCCAGGC TGGAGTACAG TGGCACTATC TCAGCTTACT GCAGCCTCTG CCTCCTGGGT 420 TCAAGCGATT CTCATGCCTC AGCCTCCTGA GTAGTTGGGA CTACAGACAT GCACCACCAC 480 ACCAAGCTAA GTTTTGTATT TTTAGTAGAC ACGGGGTTTC ACCATGTTGC CCAGGCTGGT 540 CTTGAACTCC TGACCTCAAG TGATCTGCCT GCCTTGGCCT CCCACAGTGC TGAGATTACA 600 GGCATGAGCC ACTGCACCCG GCCTAGAGAA GTTTTATGAG TGAGCCTTAG TCAGGGCTCA 660 CTGCTAAGCA GCATCAGGCT ACAGCCCTAA GTGAAGGAAA AGCTTATCTC ATTTCTGATA 720 AGATGGGATA CGTGGCAGTT TTGATTTTGG TGCTTTCCTG TGATGGGAGG CTTCAGGACC 780 TGGTTTCACC CAGGATGGAG TTTAGACACA GCATAACCCT GAGGGCATAA GGAGAGGCAG 840 GAAGCCAGAT AAGTTATAGT CGGTAAGGAT TAATTAAACA CAACCCAGGT GAGAATGAGG 900 AAGTAGTTCC CAGATAACAA AGTGGAGAAA ACCGGCCCCA GGCCTAAAGA CGTGGCAGCA 960 ATAACCTAAC AGCATGTGTG AACTGAGCTC ATGTTGGTGA CAGGACCTGT GGTTTGGCAT 1020 AGGTTTATTC CCTAAGCAAA CTCATGCAAA ACTGGGTATA CAGCACTACC ACCTTCTAAC 1080 CACAGAATTT AAAGATTAAG TATGAGATTG GTGTTGTTTA TGAGAAAGCA GAGTGTTGCT 1140 GTATTTTCTT TCCAGGGCTT GTACAATATG GGCAACATGC CTATTTGGCC TTTGCTTAGA 1200 TACTCAGCCC GAGAGATGAA CAACAGTTAT TTAGAAGACC TGCTGTAGAA GCTCTAGACA 1260 TTGTGTGATA AAACTGGAGA TTTAACACAC ATTCTATGAG TTCTGCTCTT GACTAAGCTT 1320 ACTCTCTCTA CACAGAAGTA GGCAGTTTAA TTTCAACACA GGATTTTCAC ATTATCTTAA 1380 GCTCCTACTG TCTCCTACTG ACTAAGAAGT TCTGCTATTT GAAAAGGAGT TTATTTTGAA 1440 TGTTCCCACA GTTTTAGAAT 1460
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