Tag | Content |
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EnhancerAtlas ID | HS023-16128 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr20:37625920-37627060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr20:37626482-37626493 | TGGGTGTGGCT | - | 6.14 | MLX | MA0663.1 | chr20:37626827-37626837 | ATCACGTGAT | + | 6.02 | MLX | MA0663.1 | chr20:37626827-37626837 | ATCACGTGAT | - | 6.02 | MLXIPL | MA0664.1 | chr20:37626827-37626837 | ATCACGTGAT | + | 6.02 | MLXIPL | MA0664.1 | chr20:37626827-37626837 | ATCACGTGAT | - | 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 |
GH20I038997 | chr20 | 37626014 | 37627090 |
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Enhancer Sequence | CCAGGCTGGT CTCAAACTCC GGACCTCAGG TGATCCTCCC GCCTTGGACT CCCAAAGTGC 60 TGGATTTACA GGCATGAACC ACCACGCCTG GCCAGATTCA TTGTTAATTA ATACTTACTA 120 ATTGTTCACA ATTGCCTTTT ATTGTCTTGG TGGAACACAG AGATGAAAAA AATAGCTTCT 180 TTCAGTTCTG TCTATGGTAG TTGATATAGA TGACTTTCTG GAAGCAATTT TGTAAGCGGG 240 AAGACAGCAT GTAGGAACTT TGTCATGCCT TGCTCTGCTG TGGTACGGGA CATGCTGGAC 300 CTCTGGTAAG CTGGGCCATT CCTTCTTATC CTGTCCTTGC TGCTCAGCCA GTGCCTCCTG 360 TGTGAGGGGA ACGGTGGTTT CTAAGTGTCT GTGAATGGGG GATCTGTGTG TGTGAGTCAT 420 CTCTGTGTGG GTTGTGGGTC CGTGTGTGAG GGGCCTACGT GAGGTATGGG ATGTGAGTTC 480 GTATGTGAGT GAAAGAAAGA AAGAGGATAT AAGTGGGCGA AAGAGGGCAA GAATGAGGAC 540 TATGTGGGAG TGGCAGGGGG GTTGGGTGTG GCTTAGGAAA CATTTTGATC TAGAGGCGTA 600 GGGAAGTCCA GAACTCATCC CCTGCCCCCC AGCGGCTGGG TCTGTGGGTG ACAGACTAAT 660 TTCAAACCTC CTAGAGCTAG GGCTGCTGAT AGGCCACCTG CCGTGGTTTC TCTCAGGGAC 720 TGGGGTGGCC CAGCCTGCAG ACAAAGACAG CAGTGGCTGC AGCCGGGAGG CAGAGACCTG 780 CAGAGCATGA TGGGGCTGAT CGAATAGCTG CTTTGGTTGC TTTATCTGCT TTCTTAATGT 840 AAGCCCAATT AAACGAACAA TTATATAACA TGACTGGATA TAATTATGAA GTATTTATTG 900 ATCCTGTATC ACGTGATGAT ATTGCTTTTC TTTTATTTGC GTCCAACTGC ATGGCAGAAT 960 ATATGGTTGC TGGTAGCTCC CATAGTTTTT TTGTCATAAG TCCAGCTACT TGAAGAGAGA 1020 CTAATTTCTC TTTCCAGATT CTTAGAGAAG GAACTTAGCA TCAGCTGGGG TCAGGTCTCC 1080 ACCCTGGACC AGTCTACATG GGCCAAGGCT GTTGGCCAAT CATGGGTGTG TTGGGTAGAC 1140
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