Tag | Content |
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EnhancerAtlas ID | HS182-19506 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr7:2083200-2084170 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr7:2083551-2083562 | ACAGGGTGTGG | - | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr7 | 2083256 | 2083318 | chr7 | 2084003 | 2084123 | chr7 | 2083620 | 2083837 |
| Enhancer Sequence | CCTACAAGGA CGCTGGGTCA TGACTGTTCT CTGGAGGCTA CGGGTGCCCT GCAGAGTGGA 60 GGCACGCGGA GGGCCTGGGG GGGCTGGGGA TCCAGACTGG CTGAGCGCCT GTTTCCCACC 120 ACAAACAGCC CTGCGGAGTG CCAGCCTTTT TCTCGAGAGT GGGGGCAGCA CCACCCCAGG 180 CCTCCTGCCA GGCCCCAGGG AGCCCTGAGG CAGGGGCCTC TGCCCATTCT CTCCTCCCAA 240 CACCCCGCAC TGCCCAACAT AGACATAAGC TGGGCCCAGG GCTACTGAAC AGGGCCAGGG 300 AGGGCCGGGC AAAGCCTGCC CCTGGAACGT GGCAGACCTC ACCGTGCAGG AACAGGGTGT 360 GGGTGGCGGC CGCGGGCTCG GACGTGACTC AAGCACAGAT GGGTGCCCGT CCCGTCAAGA 420 GAGCACACGC AATGGACGGC GGCAGCAATG CTCCAGCAAC CACAGCAAAG GCCTGATGGA 480 GAGAGGAGGG GAGACAGCAG CATGGGAGGA CGAGCTGCCT AGAGCTGGCG GCCACAATGC 540 GCCGCAGGAA GGGGAGCAGC CAACGGTCTG GAATAAAAAT CATAGCGAAT GCTCACAGGA 600 CAGAGGCAGC TACTACAGGT CCTGATCCAA GGGTCACTCT TGCTCATTCC TCCCAACTTG 660 TTCAGTCCGC CAACAACACT GTGAGGACAC GCTGGGACAA TCTCCGCTCT CTCCAGCAAC 720 GAAACTGAGA CACAGACGAA TGACTTCGGC TGGGTTCCAC ACAGCCAGCA CCTGGGACCA 780 GGATTTGAAC TCACGCACCC AGGCTCCTGA GAGGACGCTC CTGCCACAAA GCACCTCAGG 840 TGTGAGAGGC CAAAGAGAAG CTGCCCGGCG CACGTGGAAG AAGGTGGGGA CGCTGTGAAC 900 ACACTGGGAA CAGTGCTTTA GAAACAGCAG CAGTGAATCC CAGAGGAGCC CGCAGCATGT 960 GTGAGATGAT 970
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