Tag | Content |
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EnhancerAtlas ID | HS145-26862 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr9:117314100-117315030 |
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) |
KLF4 | MA0039.3 | chr9:117314906-117314917 | CCACACCCTCC | + | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH09I114550 | chr9 | 117312897 | 117316577 |
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Enhancer Sequence | CCTATTGAGG GAGAGGTGGG CCTTCTTCCC ATTCTCCATC TTCACCTACA AGCTATCCAC 60 TATGCAGGGG CTGCTTGGAG TTTTAACACT GATCCAGTAG CTCACCTGGC TCTTGCCTAA 120 GTAAATTACC TTTCTCCCTT GGGGTTGGGG AGGTGTGGGT CTGGGTGGTG GGCACTGGCT 180 TTACCTCCAG CTCAGCTCCT TCTCTTTGGT CCCGCCTCCC AGGGTTTTAT GTGTCCATAT 240 AACCACTGAC TCAGGGTCAG CTTTTTCCAG TCTAGTGCGT CAGCACAAGT GAGTGATAGA 300 GCCTGAAGGC CATTACTCAG GGGAGGATGG TGGTGAGTCA TCACGAGAGA CTCCTTCCCT 360 AGTCTGGCCA CTCTGCTCCA AGCTGTGCTG GGAGACAGAG AATAATAACA CCTTTTGGAC 420 TGGCCTTTTA AAAATAGAAA CAATGGAGTC TGTGGCTTTA GGAGGAGAGG TCCTGGGAGT 480 CAGAAGCTCA GTCCTGCTAG CTTGTCATTC CTTGGAGGAT GCTGGCTACT ACTTTGCCCA 540 CCGGTAATTG AGGGTGTTGC CCTTGGCCAT TTGGGGTGGG CTTTCTGAGT CTTTTAGAGG 600 TTGCAGAATC TTACATGTGC TATAAACCAA GGACACACCC TACCCAAAAT TTATATACAC 660 ATTCATGCAA AATGTGTCAT GCAATCTCAG GGTTTCATGG AACCCGCTGA CACCCAGTCA 720 TGGGCTCCTG GCAATGAATT CCTGATCTCT GGGCTCTATT TGTCTAATAA TTCTATGAAA 780 TATGTTTCTT CCAAATTCTA TACTCCCCAC ACCCTCCATA AAATCATTTT TTAAAACATT 840 TTTTTGTCTT CATTTATTTA AGAAACATTT ATTGAGTGCT ACCCACTCCT GTGGAAAAGT 900 CCAGTATTGC TGGGAGAGAG AAAAGAGGAA 930
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