Tag | Content |
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EnhancerAtlas ID | HS098-12317 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:7175840-7176890 |
Target genes | Number: 38 | Name | Ensembl ID |
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SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYB | MA0100.3 | chr12:7176059-7176069 | GACAGTTGGT | - | 6.02 |
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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 |
GH12I007068 | chr12 | 7175430 | 7177082 |
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Enhancer Sequence | AGGGCTGAGG CTTGGGGAGA GATGATAGCC ATGGGTGACT GGGAGTCACC TTCTGAAAGC 60 AACTGTAATC CTCTTGGGAA AGGACTGAAC AGTGACCTGC CAGAGTCCAG CTCAGTGAGG 120 TGGCAGTATC ACTGTGCCGT GGGCTGCCAG GGCCGTGGGG AACCTCCTCA GCCGCACTGA 180 AGCCAGGCCA ACTGGAAGGA AATAGAAACG TCAGCCAGCG ACAGTTGGTG TCTGGTAATG 240 TAGCTGCAGT GAGAAGATAC AGAACTGCTA AAAACAGGGC CTGAAAGCTG AGAGTGTGTG 300 AGTAATCAAC ACTCAGAAAC AAGTCTAGCT AAATAGCCTA GTTATTATAT TAAAAGTTTA 360 TAGGGCAGCA AGATATAGAG GAATTCAAAG AATGAGGAAG ATAAGAGTTG GGTAGCAGAA 420 GGCTGAGGCA AATCCAATAG GATAATAACC ATCCTGGGTG GTACTGAAAG CTGAAGACTG 480 AGCTGATTTG TTGCATTTAT TATCTCATTC GTGTCCGTAT AACAGCCCTG TGAGCTAGGT 540 GTCATTGGTC TTATCTGACC AATGTCAAAT GTGAATGGGT GGGGTGCAAG TTCACAGAGT 600 TAGCAAGTGG CAAAGGCAGG CTTTGAGCCC AGGTCTGTCT AAGTTCACAG CCCATTGTGC 660 TCAACTTGGA GTCCCTCCAG GCTGTCTAGT AAGGGATTTA AGTAAGCAGC TTCACTTGAA 720 TTCAGTTATT AGTATAACTG AATGGTAATG GCACCAGTCA CTGGGAGTGA GAGGTCAGGG 780 CCAAAGAAGG GACCCCTCTC TACTTCCTAG GCTGACCTGT GGTTTACTAG GAGGGACTCA 840 GGTGCAACTA GGACTCCAGT AAAGAAGGTG ATTAAAGTTT GATCTGGGCA TCTGAAGAAG 900 GCAGAAATCT TTCCTCCTCC ACCATCTGTG TGAGAAAAGG GTTTCCAGCA CTGGCTCTTG 960 ATTGGGCACC GGCCTCATGT GCCGAGTTGG GAGGTGCAAA GGGGACCCCT GCCTCCAGGG 1020 GGGCTGTGGG TCGCACTGTG GATAGTGTGA 1050
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