Tag | Content |
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EnhancerAtlas ID | HS162-02855 |
Organism | Homo sapiens |
Tissue/cell | Plasma_cell_myeloma |
Coordinate | chr13:98199910-98201280 |
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) |
STAT1 | MA0137.3 | chr13:98201091-98201102 | TTTCCCAGAAA | - | 6.02 | STAT3 | MA0144.2 | chr13:98201091-98201102 | TTTCCCAGAAA | - | 6.32 | Stat4 | MA0518.1 | chr13:98201088-98201102 | TCATTTCCCAGAAA | - | 6.62 |
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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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Enhancer Sequence | CCAAGCCTTT CTTATTAGGT ATCTTAGTCC AGGCTGCTCT AACACAATAC TGTAATGGGT 60 GACTTACACA ACAGACCTTT ATTTCTCACA GTTGTGTGGG CTGGGCAATC CAAGATTGAG 120 GTGCTGCCAG ACTGGGTTCC TGGTGAGGGC TCTCTCCCTG GCTTGTATCT TACTGTGTGT 180 TCACCTGGTC CTTCCTTGGT GACAAATTGT AGAGGAGATA GCAGACATAT ACAACTAAAG 240 AGGGTAGCCA AGCTTTTAAA TTTTTTTTTA AAAGTCATCT CTCTAGACAG AATATACATA 300 TGTGGTTTTG TAGCTATTTT TTACTAGAGA TTATAAACAA AGGTAGCTGT AAAGCAATGA 360 ATTCTCAATT CACTATAAAA GTTTTGGAAG CACCATTTTA TGCTAGGGGA AGTCCTAGGC 420 ACTTGAGTTC CTGTCCCCAG GGATGTTTGC AAGCAAAATA TGGACAATTA AAATATAGTT 480 GTATAATAAA GATATTAATA AAATACAAAT CACCATTTCT TTTGTGGGGG TGAAGGTGGA 540 ATGGGTGCTA TATTGAAATA TTTTTACATA TTATAAAATG CCTCATTAAG AGCCTGTCTT 600 TTCCTGCACC TTGTCTTCTA CTTCCTGCTC AAAAGTAGCA TATGAACTTC CTATTTCTGC 660 CGGCAAGTCA GGTGAGAAGA GAAAATGAGT TTATGAAAGT AGGCATGTGT CAGTGCTCTC 720 TGAAAAAGAC TTGTCTGTAT GCTGCATCAG CACACACCAT CATCAAAAAG CAAAGCAAAG 780 CAGGATCGAT TTTATTTTAG TGTCTGCGAT TTTAAGGACA ACAGAAAAAC AACAAAAACC 840 TCACATGTAT TATATCATGG AAGTCTGCCA ACCCTCTACC AACAATACTA TTCTCATTTT 900 ACAGATGCTG AATCTGAGCA TCAGAGAAGT TAAGGCACTC GATAAAGACT TCAGTGATTT 960 TTCCAGATAA TACAGGGGAA GAATTGGAAC TTAAAGCCAG GTCTTCTGTC TCCAAATCCC 1020 ATGACCTTTA GAGCATGTTT GAAGGAGAAA GTTCACACAT TTTCATCTGA GATACCTACT 1080 ACTCTTTCTA AAACTAAATG CGGAGTCTCA GCTGCTTCTA TGAGCTGGTA AGGGTGCTGT 1140 CGTGGCTTTG TGACATGTCA GCTTGGCTAG GCTGAGCTTC ATTTCCCAGA AATCCCTCCC 1200 TGTATGTTTC TGGTTTGGGT GGGTCAAAAG AAACATTCTG GAGGCAGAAG GGGAGGAGTA 1260 GCCATTCTGT AGCTCACAAA GATTGTTACT GATCTGCTGA CTCGCCTCAG TGCTCTGGCG 1320 CAGCAGCTGA GGCTGCAGCT CTTCTCCCTT CTCATGGATC CTTTTTCAGC 1370
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