Tag | Content |
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EnhancerAtlas ID | HS108-06771 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr11:3112260-3113660 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr11:3113176-3113195 | TGGCGCCACCTGGTGGCCG | - | 9.51 | ZEB1 | MA0103.3 | chr11:3112598-3112609 | GGGCAGGTGGG | - | 6.14 | ZEB1 | MA0103.3 | chr11:3112640-3112651 | GGGCAGGTGGG | - | 6.14 | ZNF263 | MA0528.1 | chr11:3113576-3113597 | GGAGGAGTGAGGTGAGGAGCG | + | 6.03 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 3112376 | 3112420 | chr11 | 3112489 | 3112539 |
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| Number: 2 | ID | Chromosome | Start | End |
GH11I003092 | chr11 | 3113101 | 3113430 | GH11I003091 | chr11 | 3112881 | 3113030 |
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Enhancer Sequence | GAGGGTGGTT CTGACCCCTG AGCCATGAGG ACAGATGAAA GCCGAGGCCA CTGTGGGAGC 60 TGGGAGGTTC ATAGGAACCC CAGATGGCTA GGGTTCCCCA TGTCAAGGGG CATCTCCAGG 120 GGGGAACCCC CACACTCAGC CGGCTGCTCA CAACCCCAGG AGTGCAGGCA GGGCTCATCC 180 ATTCAGCCCT TACTTGAGCT CACAAGGAAC CCAGGACAGG AACTGATGCT CAGGGGTGGG 240 GAAAAAGCAG AACCTGGCTG TGGGACCACC ATGTAACAAC AGGCGTTTGG GGCCAGAGAG 300 GTGCCAGGGA CGCTCTGCAT TGGGTGTGGT CAGCGACGGG GCAGGTGGGG TCAGAGCCAG 360 GACAGGTGGG GTCAGAGGCG GGGCAGGTGG GTTTGGCCAC AAGGTACTCC ATGGGATGGT 420 TTTTGAGGCA TGGCAGGGCC CAGGCTGACT GACCTCAGCA GGGGCTGCGG GGTGGGAGGC 480 TGCAGAGGGC ATTGGGGGTG GACATCTGCT GGAGATTGGT GGGGAGAGGC TGAGGAGCGG 540 GACTGCGAGG GTCTGGGGCC AAGGGAAGGC AGGAGCTAGC AGTCTGGCCT GAGCCCGGGG 600 GGATGGAGAC TGTGCTGCAG ACATAGGGGG TGCATCTGTC TACCTTCCTG AGGCTTCTTC 660 CCTAGTCCCT TGGCAGGCAG AGCATGGGAC ATGCAGCCAA GGAGATACCG CGGCCCCCAG 720 CTTGCTGGAG AAGTTAGGGC CATCAGGCAA GCAAGGCCTC TCATCTGAGT CTGGCCCAGA 780 CGGCATCAGC TGGGGAACAC GCCCCCATCC TGTCCGCTGC GGGTGAGCAC CGGCCGCGCT 840 CTGCACCCTC TGCACGCAGT AGGTGCACGG CTGGGGCGGT GCAGCTCAGC ACACCTGGAA 900 CGGGGGCGTG TGGGTTTGGC GCCACCTGGT GGCCGCCTAA GGCATGGCAC CAAGACACAC 960 CCAAGGCAGC TTCCTCAGGT TACTCCCTGG AGCCTCCTGC TGTCCCGCTT CCCCTTTCCA 1020 GACACAAGAT CTGTGCAAGT GCTGGCTCCT CCTCCTCCTA CCTGGGAAGG GCCCTGGGCT 1080 GCCCTGACCT TCTGTTTCCT GATCAGTGGA ATGGGATAAT GTGGCTGCTA ACTTGGCAGA 1140 GGGAGACTTT GGGGGCAGTG GACAGAGACA GTAGACACAG GGTCCCACAA GCCAAGGTGC 1200 CCCTAGAACT GAGCATCCTG CAAATCCCGG TTTCCTGAGT CCCATGCTCG GCAGAGAAGG 1260 AAAGGGGACG AGGGGGCTGG GGGATGAGGG CGTGAGGGAA ACGGAGCGAG GGGAAGGGAG 1320 GAGTGAGGTG AGGAGCGAGG GGTGGTGGTG GCCACACGTG CAGCTAAGAC CAGCCCTGGG 1380 TGGGGCCTGT GGGGTGCTGA 1400
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