Tag | Content |
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EnhancerAtlas ID | HS087-04677 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr11:125273860-125275240 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
INSM1 | MA0155.1 | chr11:125273898-125273910 | TGGCAGGGGGCG | + | 6.07 | ZNF263 | MA0528.1 | chr11:125273903-125273924 | GGGGGCGGAAGGGGTAGGGGG | + | 6.03 |
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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 |
GH11I125403 | chr11 | 125273578 | 125275510 |
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Enhancer Sequence | TGCCTATTGA CCTCTAAGGA ATTTTGGATT TTCCAGATTG GCAGGGGGCG GAAGGGGTAG 60 GGGGCCATCA CCTCAGCCAG GACCCTAGAG GTTCTGCCCA GTGGCTAAGC ATCCTGAGGA 120 CAGGACCAGG GAGAAGACTG GATGGGGCTG GGGTAGGGGG CAATCTACCC TGGAAAGATC 180 ACTACTTAGA TGGACAGGGG GCATCCCTAG ACTGAAGTGG AATAAAATGA GCCACACTGC 240 CTGTCACAGG CATTAAAGCT GTCTCTTCTG CCGGTTCCTC ACCCCCAGCC CTGCAGCCGT 300 GGAGCCCAGA GACCAGAGGG TGGCCTTTGC CGCCAGGCTA GTGAAACCTG AGCGCTTCTC 360 CCGCCTGAGA AGGAATGTTC CTTAAGAGCA GCAGCTGCTG CTTGTCCCCA CAGGCCAGAA 420 CTGCCTTTCC CTTGAGACCA AGGCCCCCAA CAGGAGTGGA ACAAGAACAG GATTAGGTGG 480 CTTGTTTACA TGTGCTTGGC TTTCCCGAGT TTGGGAATCT GGCTTTTCTT GGTCTAAGAC 540 AGGGCCCTGG CTCTGCCAGA ACGGAGGGAT GCTGCCGGGA AGGGGTGTCT GGGGACAGGG 600 ACAACCTCTC CACCCTCCTA AGGCACATTT GCGCGGGCAC ACACACAAAC ACACACATCA 660 CACACACACA AACACACACA CACCACCACA CACAGGAATA CACCCACAGC CTTAGGCCAA 720 AGTCAGACCA CACATGTATC TCGCATGTAC CATGCACTTA ACATTGCGCT AAGCAGTTTC 780 GGGGAATTCA GAGAAAGACC CCTCTTTCCC TCAAAAAGCC TGCCACCAAG CTAGGGAAAG 840 ACGACGCCTG CATTAGAGAG AACCATTCTG TTGTGTCCAG TATGTAAGGC AGATGGGAGG 900 CTTTGAAGAG TCCAGAGGAC GGGCCGCGGC TGTGCCCTGG AGAGGTCAGG ACAAGCTTTC 960 CAGCAGAAAG GAGACATTCA GAACCGACCC CCACCCGCCC CGAGCCCAGG CAGGGGAGCC 1020 GCCAGCACGC GCCTTCTGGG AGGCTTTGGT GAGTGTGGTC TGAGCCGGTG GATCAGCAGA 1080 GACCTCTAGT GGCCGGGGGG AGGATGGCAG GTGGCTGGGG CTGGCTCCGC ACTGCACCCC 1140 ACTCCGGCCA CCGACTCACC GTCACCCACC CTCCCACACA ATCCTTAGGA AATGGCATGG 1200 GCTCTTTTAC AGTCCTCAGC TGGAAGGATC TTTGCCAGGC CATCCCGTTC ATTCCCCTGT 1260 TTCACAGGCA TCCAAGTAAG ATAAAAATTC CACCTATTTC AAAACAGCTT AAACAGAAAC 1320 TTTTCTGTCA TTTATCTCCT TCACTCCTTC ATGTCTTTGT CCCATTCTGG TTTCTTCCAG 1380
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