Tag | Content |
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EnhancerAtlas ID | HS165-03777 |
Organism | Homo sapiens |
Tissue/cell | Ramos |
Coordinate | chr12:122275070-122276410 |
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) |
GLI2 | MA0734.2 | chr12:122276194-122276209 | CTGCGTGGGTGGTCA | - | 6.46 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 122276121 | 122276401 | chr12 | 122276179 | 122276200 |
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Enhancer Sequence | AGAGGCGTGA TCTCGGCTCA CTGCAAGCTC CACTTCCCAG GTTCAAAGGA TTCTCCTGCC 60 TCAGCCTCCC GAGTAGCTGG GATTACAGGC ACCCTCCTCC ATTCCCGGCT AATTTTTGTA 120 TTTTTAGTAG AGGCGAGGTT TCACCCTGTT GGGCAGGCTG GTCTCTAACT CCTGACCTCA 180 AGTGATCCAC CTGCCTCAGC CTCCCAAAGT GCTGGGATTA CAGGCATGAG CTACCGCACC 240 TGGCCATATG TGCCCAACTT TCTAAAATGT TGACTCAAAT TTGTTTGAAA CCATGCAGGC 300 AAAACGAAGT AGGTCTATGA GCCACATTTG GTCTGTAAGC CACTAGTTTG CATCCTTCTG 360 GGTTATACAA TTTCCCTTCT TCACATTAAG TCACAGGAGA ATAGAGGGGG AGTATTTTTT 420 TTGCACGGAA TCCTTTGGGT TCTCTCTGAT CTCTTTATTT CTGAAGTTCG TGATCCCAGA 480 AGCTCTGATT TCTTCTATAA TCTGAAAAAA ATCCCCAATT CCCACCATTA TACCAACTCA 540 GAGTATTTTT TTCTTCTATT GAGCTCTGCT GCCTCCTAGC TCTGAGTTGA CTTATCCTCA 600 CGGAGGGTTC TCAAGCATTA GAAGCAGAAA GAGGCCAGAG ACAGTGGCTC ATTCCTATAA 660 TTCCAGCACT TTGGAAGGCT GAGGTGGGCG GATCACCTGA GACCAGGAAT TCGAGACTGG 720 CCAACATAGT GAGATCCCAT CTCCATGAAA AATAAAAACA AAATTAGCTG GGCGTGGTGG 780 CACATGCCTA TAGTCCCAGC TACTTGGGAG GCTGAGGTAG GAGGATCACC TGAGCTCAGA 840 AGGTGGAGGT TGCAGTAAGC CAAGAGCACA CCACTGCACT CCAGCCTGAG CAATGGAGTG 900 AGACTCTGTC TAAAAAAAAA AAAAAAAGAG AGAAAAAGAA AAAAAAAAGA GGCCAAATTT 960 GCCCACCACC AACTCTTACC TGGTTTTGAA GAAAGAATCT CCTTCCTAGG GTTTTAGGAC 1020 CCAGCTGCCT CATTCTTTTG CAAGGATCAC TCACTCTTCT ATGAGTATGA ACAAGCCCCT 1080 TTCCAAAAGA AGTCCTCACT GCGGGCAAGG CTGGGGCAGT GCAGCTGCGT GGGTGGTCAT 1140 GGGCACTGCC CTGCTGAGGG CAGGGACTGG GATACCAGGC CCCTCCTACC TGCTTTATCT 1200 CTGAGACCAG GAACCAAGGG ACCATATCCT ACAGTTGATG AGCAGGGATG CTGCCCCTAG 1260 AGTCCCTTGT CTAACACTCT CCCCTCTCCT GTGTTCAGAG GTTTGGGCTC TGGGTAGCAA 1320 AACTGAAGAC AGCTCATCTT 1340
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