Tag | Content |
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EnhancerAtlas ID | HS108-07945 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr11:68565620-68566680 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr11:68565875-68565894 | TAGCGCCACCTGCTGGTTC | - | 7.1 | ZNF143 | MA0088.2 | chr11:68565857-68565873 | CACCCACCATGCCACG | + | 6.05 |
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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 |
GH11I068798 | chr11 | 68565801 | 68565990 |
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Enhancer Sequence | GCAGTGCCCC CCAACCACCT CACAGCTGCT GTCCCTTCAC AGCCTGCTGG ACCCAGGGAT 60 CGCTTCCTTT CAGCTTTGTG CTGAAACACA CGTACCTACA GAACAGTGCC CATGCAAGGG 120 CCTCGTGTGC GGAGAGCTGT GCAGAGAGCT GACGTTTACC AGTCCAGCAC ACCGGTGCAG 180 CCAGCGAATA TGCCCGGCCC CCTGAGGCTA GAGAGACCCC TCCAGGCACT GCCCATCCAC 240 CCACCATGCC ACGTCTAGCG CCACCTGCTG GTTCTGTCAG GGTCGCTTTG GACACCTTCT 300 CTTCCGTGTT AGTTGTTCCT CAAAGCTAGA CTCCCTCCCT TGCTTTGTCT GCCGGAGGCC 360 TGCTCTTGCC CTCCCAGTAC GTGGAAGCCC AGCCAGCTCC CCGCACACAG GGTGCCAGCT 420 AAGACGCTTC GTTGGAGGAG ATGCTCCTGG GACCACCGAG CCACACTCAA CCCCAGGGAG 480 GGGCGATCAG CACCGCCCTA TCCCACACCA TCCCTGCATC CACCAGCGAG CTCGGGAAGG 540 ATGCCCTTGG AATCAAGATA AACCAAAGAG GAGGATGGGA GCAGGTCTCT GGGGCAGCAT 600 GGCACTGCTG CAGGAGAAAC AGCTCACGGG AGGACTCTCC GGGGAAGAGG GAGAGGGAGA 660 AGCCTCCTGC GTGCAAAACA CAGCATCGTG CTGGTGTACC TGCACTCAGG GTAAAACTGT 720 CACTGTAGGC TGGGTGTGGT GGCTCATGCC TATGATCCCA GCACTTTGGG AGGCCGAGGT 780 GGGAGGATCA CTTGAGCCCA GGAGTTTGAG ACCAGCCTGG TCAACATAGT GAGACTCTGT 840 CTCTACAAAA AAATCCAAAA ACCAAGAAAC TGTCACTGTA ACTACACGTC AGTCCTAACA 900 CACACACACT CCACTCTGCA CAGAGGTAAA ACTATAGCTG GAACTTCCTA GGGTGTGATT 960 TTGGCTAATC CAAACTGTCA TTTCAGCCCT GTTATCCCTG CCCCTCAAAA TTAGCGTCTT 1020 CATACGGAAA AATTTCATCA AGAAAAACTG TGTATACAGA 1060
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