Tag | Content |
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EnhancerAtlas ID | HS101-30643 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr3:127830960-127831730 |
Target genes | Number: 14 | Name | Ensembl ID |
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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) |
JUN(var.2) | MA0489.1 | chr3:127831448-127831462 | AAAATATGACTCAT | + | 6.42 |
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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 |
GH03I128111 | chr3 | 127830362 | 127833950 |
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Enhancer Sequence | TGCCAGCAGA AATGGGGCCA AAAAACTGCC CCAGAAGTCC TAGCTAGCAA AAAGCAAAAA 60 TTCGAAAGAG AAGCCATTTT CTTCTCACAG CCAATCTTCA CAGCAACGGC TCTAGAAATG 120 AGAAAGATGT CGGATCAAAC TACTTCTGCC ACTTACTAAC TGGGTCCCTA GCAAGTTATT 180 TAACCTTCTG AGACTGCTTC TTCAAATGCG AAATGTAGAT TGATAATCTC CCCTCAGAGG 240 AGGGAAGGCC TGGCTCATCA CAGGCACTCA CTATGATAGC CTGAGGCCCT AAGGGTTAGG 300 CGCCATAAGC CTCTAAGCTC TGCCAGTCCC CACTCCTCAG TCTCCTCACT CTATGACAGG 360 CCACAACTCT TCTGGCTCGC CATCCAGGAC CAGGGGCATT CTGGCCACAT GGCACACAAA 420 GATTCTGGCT TGAGTCCAAA ACCTTTTCAG TGGATAGTCA TCTCTAATGG CAAAATAAGA 480 CTTCCAGGAA AATATGACTC ATTAAAAAAA CACTTTTAGA CACATCTATT TATTGCATGA 540 AGAAGCGCAG GCTCACAGCT AGGGTCCATA GTTGCTCCAA TTGCTAACGC ACTTCAATGA 600 GAAAAACTGG GGTTTTGTTT TATTTGAAAA ATAATGCACT ACTAAGTGCC AAAAGAAAAA 660 CAGCAGTGCC ACGAATACCA GTCATAAAGG CATCTTCACC ACAAAGAGGC TTCGGTGCAC 720 AGGCTTCAGG AAGTGAGACC AACTCCTCCC ACAAATGTGA CACTACTTAC 770
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