Tag | Content |
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EnhancerAtlas ID | HS182-16265 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr3:125847820-125848660 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr3:125848270-125848285 | AGGTCACCCTGGCCA | + | 6.25 | KLF5 | MA0599.1 | chr3:125847872-125847882 | GGGGCGGGGC | - | 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 |
GH03I126129 | chr3 | 125848461 | 125848610 |
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Enhancer Sequence | TCTGACCACT GCCCCATAGC AGGGTTTCTT GGCTCCCACA CTACTGACAT TTGGGGCGGG 60 GCAGTTCTTT GTTGTGGGGG GCTGTACTCT ATCACCCCCT CTGATGGGAC AACCAAAACC 120 ATGTGCAGAC CTTGCCCGAT GTCCTCTGTG GGGACCCTGG AGGCGATGCC TCCACCTGCA 180 GCCTGGCTCC TCTCTGGGGC TCTAAGGGTC CACAGCCCAC TTTCCCACAG GAGCCTCCTC 240 CAGCCCGTGC TTGAGGAGTT GGTTGTTCAT CTGCATGAGC TGTCAGTGAC ACAGGGACAT 300 TGGAGCACGT TCTCCTTGCA AATACTCCAA CATTCAGGTG GAGCTGAGGG GCCTTTGGCC 360 ATGCCCACAG CTGTGAGGTC CCCTACCCTG CAAGGGGCAC AGAGCAGGTG GGAATGACTG 420 TGGTGCTCAT GCCAGCTGGG CCCTGCTCCC AGGTCACCCT GGCCAGGCTC TCCTGTGGCA 480 CCGCGTGCAG GCGCAGTGAG GGTGGACCCA GGGCTGGGGC TCTCTAGGTC CAGTTGCAGG 540 CGCATCCTCA GTGCAGATCA TGGATCAGGG CTGCACCAGC ACCTGCTGCT CTGGTGTTTG 600 CTGTCACCGG CCTAGCACAG TGGCCATGCA CTCTTGGGTA AGCCTCCTCA GGCACGCGTG 660 TGAGTAACTC ACCAGGACTG GGGCCAAATC AGGATGTATG GCCTCGAGAG GTCACTGCCC 720 AGTTTCCTCT AGCAGGGAAA ACCCAGAGCC CGGTGGCTGT GTTCCAAGCC CTTCTCCCTA 780 CTCCTGCCCT GGGGCCACTG GGTGGCGAGG TGAGGTGCCT CACGCCAGGT TCATTTCCCG 840
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