Tag | Content |
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EnhancerAtlas ID | HS105-76451 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr8:11499140-11500620 |
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) |
KLF14 | MA0740.1 | chr8:11500516-11500530 | GGACACGCCCACTC | + | 6.43 | SP4 | MA0685.1 | chr8:11500514-11500531 | CAGGACACGCCCACTCC | + | 6.46 | SP8 | MA0747.1 | chr8:11500517-11500529 | GACACGCCCACT | + | 6.37 | ZNF740 | MA0753.2 | chr8:11500218-11500231 | CCGCCCCCCCCCC | + | 6.64 |
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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 |
GH08I011640 | chr8 | 11498236 | 11501093 |
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Enhancer Sequence | TTGCTTCATA TACTGGTTTT GAGTGTTTAA GGTGAGAGTG AACATGGCCT TTCACTCCAT 60 GTTGGCTGGA GCTGGAGGTC AGTCCTGCTT AAACTTTTAG AGCAGAGAGC TCTTCTTCTT 120 CCCTGGGCCT GGACCTTAGA GGACGCCAGG GATCCGAGTG GCTCTTGCCA TTTTACCTCT 180 TCAAGGAGCC TGAATCTAAA GCCAACACAG CAAAAGGCAG ACCCAGGAGG TGGAGAGAGA 240 TCAGCTGCAG GTGACATCCT TGCAGCCCTG AATCAAGCTT GTTCACTAGA TTCTTAACTA 300 CAAGAGACAG AGAGGAAAAC AAAATCCCTT TGCTCAGGTC AGTTGGAGTC AGGGTTTTCT 360 AACATTTTTG CAAGCGAACA AGTCTCAAGT GATTCGCTCT ACTGTTTAAA AATGCATATG 420 ATGACGGCAT GTGTGTACCG AGCTGGGGCA GAGGTTAGAG AAATTTAAAA ATGCGTATGA 480 ATAACAGCAT GTCTCTACAG AGCTGGGGCA AAGGTTAGAG AAAGCGATCT ATGTAAACGA 540 GCTGCCAGGC CCGTACACAG TAGGTGCTCC GTGAAGGCTG TCTCCCTGCC CCGTCCTCAA 600 ATATCTGCTT CTTGATCTGG GCTTCAAAGC TGATCCCATT CTCTCTCCAG TCACCTCTCA 660 AACTCCTCCT TCTTTTCTGT TAAGTAGCAA GTCTGGTCTT TCCTTCTTTC CGAGCAGAAC 720 CCAGGCTTTA CAGTTAATAT CCTGCCGCCT CTGATTGCAG CTTTAAGAGG TGTAACATTT 780 GATAAGCTCC ATTTAGCTTG GCTGAGCTGC ATTGTTTAAA TTATTCGAAG ACAGATTGCT 840 CCCTCCCCCT ACCCTGAGGA TTTCTGCTCT ACTGAGCTTG CCCACAGCAA GTTACCAGGA 900 AACACGGCAG GGAAGTCAGC AGGGCAGTTT GTCACCGTGA GGCTGAAAGT CAGTTCCAGC 960 CGCTGTTCTG CAGCCATCAC ACCCCATTAT TCCCTGCTAA TTGCAAGCCT GGTATGCAGG 1020 CTAACTCTTT GAGAACAATG CCAGCTTTGA TTGCTGAAGA GGCTTATTCC TCTCCGCACC 1080 GCCCCCCCCC CCCGCCCCCG CCCTCTTCTC CCACCGTCCT CAGCTGACTC TGCCTGTCTG 1140 GGATTCCAAG CATCTCACAC TGGGGAAGAA GAGTCTGGGT TGGGAAGGAA TCTGAAGTGA 1200 AGCCCGTTCC CCAGGCATTC CGATTGGGGG AGGGAAGGAG GGCACTGAGG GGAAGGCTGG 1260 GTGGGTCCCA GCCCCCTGAG ACGTGAGCAG CCTCCATTCT AAATGATGTG GAAGAGCCGG 1320 CAACCCAGAC ACAGCTGCTC TGCAAGCCCA TCTGCCCAGC TCAGGGCTCA ACCTCAGGAC 1380 ACGCCCACTC CTCCTGGTCC AAACGAGGAT GGAGCCCCTC GAGCCTGTGC TCATGGGCAC 1440 TGTCTCACTC CATCCGAGCA CTGCTTAAAA CACACTGGAT 1480
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