Tag | Content |
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EnhancerAtlas ID | HS136-18251 | Organism | Homo sapiens | Tissue/cell | Monocyte | Coordinate | chr7:66282000-66283130 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SPIB | MA0081.2 | chr7:66282529-66282541 | AAAGGGGAAGTG | + | 6.07 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr7 | 66282321 | 66282529 | chr7 | 66282302 | 66282400 | chr7 | 66282400 | 66282794 |
| | Number: 1 | ID | Chromosome | Start | End |
GH07I066817 | chr7 | 66282189 | 66282986 |
| Enhancer Sequence | ATGTCTTTAG CTCCACAGAC TCCAGAAAGC CCTGTCCAGA CATGAATCAA CCTTCTTTAT 60 CATACCACAC TGCTTCTAAA GTCTCCATCT TCAGCACAAC TTGTCCTGTT AGAGCAAGCC 120 TGTTGGGGGG CTGGGGTTTG TGGTGGGTAG AGGACACTGG GAAAATCATG CTGGCCAGAA 180 GGGGGCTGTC GGGGGATGGC AGGGTAGGCC ATGGAGTGGA GAGGTAATGA GCTCTCTGTC 240 ACAGGGGTAA TCAAGCAGCA GCACTGAGGA GTCTCTGCCT GAGAGTGAGC CCAAAGGCCA 300 AACTCTCAAG GAGGGCACCC CTTGGGTCCC CAGTAGATGA GGATTTGGTG CCTGCTCTGG 360 CGGTGGGCAT CTCTTAAGCT TCTGAACAGT GCCAGGCACA GAGCTGGGGT CACAGGGCCA 420 GGGCTGGGAG GGGGAAGCAT AACCCTGCCT TGAACCACAG TCTCAGGAGC TAGAAAAGGC 480 TTCGGACTGC ATTTGGGCCC CTCCTCTTTA TGGGAGAACT CAGGTTCTGA AAGGGGAAGT 540 GACTTCCCAG CAGTAAACTT AGAGAGGCAG AAGCTGGGCA GAGCCCCTGA GTCCCAGGCC 600 AGAGTAGCGA CAGTGCTTCC CCTTAAATAG CACAGCCGGC TGCCAAGGCC ACAGGGAGTA 660 ACAGGAGGAG CTGGCCTCAA ACCCACCAGA CAGCCTCTCC CGTCGGCCAC TGCGCTGATC 720 TGCCTCCTTT TCCAAATGAC AGGTGTAGAA AGCCATCGTG ACTTTAAAAA GTGCTCAAGG 780 CTGGGCATGG TGGCTCAACC TGTAATCCCA GCACTTTGGG AGGCTGAGGC AGGGGGATCG 840 CTTTGAGCCC AGGAGTTTGA GACCAGCTTG GGCAACATAG CGAGACCCCT TCTCTACAAA 900 AAATGTAAAA ATTAGCCAGG TGTGGTGGCG TGCTCCTGCA GTCCCAGCTA CTCAGGAGGC 960 TGAGGCAGGA TTGCTTGAGC CCAGGAGTTT AAGGCTGCAG TGAGTTATGA TTGTGCCACT 1020 ACACTCCAGC CTGGGCTTCA GAAAGACCTG TCTCTTAAAA CAAATGCTCA TGGCCAGGCA 1080 TGGTGGCTCA TGCTTGTAAT CCCAGCTACT CAGGAGGCTT AGGCAGGAGA 1130
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