Tag | Content |
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EnhancerAtlas ID | HS139-17058 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr14:75374230-75375550 |
Target genes | Number: 19 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr14:75374773-75374794 | GGAGGAGACAGGAAAAGAGAG | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 75374887 | 75375271 | chr14 | 75375317 | 75375397 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I074907 | chr14 | 75374104 | 75374503 |
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Enhancer Sequence | TGCCTGGGAG GACACAGGGA AGGGCCTCTG AGGAGGCAAC CCCAGGACCG TCTACACTCC 60 AGTGGCAGCC AGGATTTTTT TTCCCCATGT CACAGCCCAT GAGGAGGATG ACAATAATGA 120 TAGTTGCTAC AGCCAGACAC AGTGCCTGAT GGCTAAGCAG TGCCTTTATG TTATCCACGA 180 AAGGCAAGAA ACAGGCCCAG AGAGGTAAAG GGACTTGTGC TGAGTTCAGG GTTTGAACCT 240 AGGTCTCTTG GCTCCAAGCT TGCTAGAAGC AACTATCTTG GGTTGCAATC AGGGCAGGCA 300 CTCTTGGGAA TAGTGATGGA ACTTGTCTCC TTATTTTAAA AATCCACACG GGCTGTTCAT 360 TTGGCAGCAG GCCATGGCAT GCTACCATCG GGGCCAAGGC AGCGGCGTGG CAATAAAAGA 420 AAATAGGACC TCTCCACACC CCAGAAAGGC ACAGCTTTGA GGAGCAGAGG GTCTGTCTGG 480 AGGGAAGTAT GAGCTTCCAG GAACCCCCAG GAGGAAGGCC AAGAGCTCTG GGCTGGAGAG 540 GTGGGAGGAG ACAGGAAAAG AGAGAGCCAC TCTGGGGGAA ATTGCAGCCA GGACTTTCGG 600 GACCCCGTGC CATGGGACGA AAGCAGGAGG GAGCCTGGAT GGACTGGTCA GCTCTGGACT 660 TCAGTTCACG CTGCATCCAT TTCGGCTATT TCCTGCTCAA ATGCAATTTG GCCTCCCCCT 720 TGCTGCCTAC ATAACTGGCC TCAGTTGCAG TGTTCAGCTC ATGAGGGGAG GACAGAAGGC 780 AGAGCCATCA ACTGTTCCCA AGAGTGCCTG CTCTGATTGC AACCTGCAAA CACAGGTTCC 840 CGGAGTGTTT GCAGGGGGAT CTTTTGAGCT CTTGGCTGAC CCAGGCTGGA CAGGGCAGCT 900 GCTTGCCTGG GTGAAAGAGC CCCTCTCTCC CATCCTCCAG CTAAGGTCTG GGGGTGACAG 960 CCAACGAGGT CATGGGTGGG AGGAGTGAAC AGCGGGCTCA GGATGATTGA ACAGCCTTCC 1020 AGGGAAGAAG GGCTGTGTCA CATTCCGCGC TTCCTCCAAA TCTGACACCA CCTGGGCCCA 1080 GGCTCTCTGG CAGAAACCTT CCCTGACCAT CCCACTCTAC TCGTATTCAT AGAAGTTGAC 1140 AGTCTCCTTA GCTATAGCCA ACTAATGTGT TGGGAGTGCT AAGTGTGTCC CTGGCTTCGG 1200 GGGCAGTTGT GCTGGTAGGA CAGCCAGGCA GTCTCTGCCC AGACTGGCTG GATGGACTAA 1260 GCCTGGCCCA TCCCACACTC AGTGGCACCC ACCAGGGCAC TACACCCAGC CCAGCCACTC 1320
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