Tag | Content |
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EnhancerAtlas ID | HS182-17822 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr5:138236360-138237840 |
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 | chr5:138236444-138236458 | GTGAGTCATTTCCT | - | 6.62 | Sox3 | MA0514.1 | chr5:138237804-138237814 | CCTTTGTTTT | + | 6.02 |
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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 |
GH05I138899 | chr5 | 138235571 | 138237772 |
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Enhancer Sequence | GTAAAGGTAG AGCCTTCCTA AAAGACTGAA AAAGTTGTCT GTCATGTACA GATGTCTAAT 60 CTGTTGATCT GACACAGGGG GGCTGTGAGT CATTTCCTCA ACAGCTCAGA TTTGAGCTTG 120 GGTTTTCCTG AAACCAGCAA AACCCAAGGC CGATTGTTTA AATGTTTTCT GAAACCTGCT 180 CTTCCGCAAG GTCCAAACTT CCACACAGTA GGCACAGATG GTACAAAAGA GGGCTGCCTG 240 ATCTCAAACT AGTGGTTGTG GTGTCAGTCT TAGCCTACCT CTTCGAATAG TGGGAATCAG 300 AGACATTTTA GTTGTTAATA CAAGTAACTG TGGTAGGAAA GATAATAATT TATTCTCCTA 360 ACAAATCCAG AGATACTTCT CACTGTTCTA CGAAGTCTTG GCTCTGCTGG GTTCTCTGTG 420 GAAGTTAACT GCTCCAAGTG TTTTTCTTTT CTCTTCTCTT CTCTTCCGCT CCCCTCCCCT 480 CCCCTCTTTT CTCTTTTCTC TTTTTTGAGA GAGTCTCGCT CTGTTGTCCA GGCTGGAGTG 540 CAGTGGCGCC ATCTCAGCTC ACTTCAACCT CCACCTCCTG AGTTCAAGCA ATTCTCATGC 600 CTCAGCCTCC CAAGCAGCTG GGATTACAGG GGCGTGCCAC CACGCTGGGC CAATTTTTGT 660 ATTTTTAGTA GAGGTGAGGT TTCACTATGT GGCCAGGGGT GGGTCTCCCA ACTCCTGGCC 720 TCAAGCAGTC CGCCCACCTC GGCCTCCCAA ACTGCTGGTA TTACAAGCAT GAGCCACCAC 780 ACCCAGCCTC TTTCTTTTTT TGGGACATGG TCTTGCAGTC ATGGCTTGCT GCAGCCTCGA 840 CCTTCTGGGC TCAAGCTATT CTCCCAACTC AGCCTTCCAA TTAGCTGGGA CTATAGGTGC 900 GTGCCACCAC ACCCAGCCAA TGAAAAATTT TTTAATGTAT AGAGATGGGG TCTTGCTATG 960 TAGCCCAGGC TGGTCACAAA CTCCTAGCCT CAAGTGATCC TCTTGCCTTG GACTGGAAGC 1020 CACTGCACCC AGCTCAGAGT GTTTCTCATT CTAACCTCAG GATCTTCTTT AGTCTCATTG 1080 TTAATAGTTA CGTCATTCTA GAGCCCCAGA TTTTCCACAG AAAGAGGCAT TTAGGAAGCT 1140 CCTCTCCTCG CCCTCTCCTT TCACTGTAGT CAGGCCTGAC ACTAGTATGT GAGGTTAGCC 1200 TCTCAGAGAG CTATGGTCAT GATGTTGCAT TTGCACATTT GTCATTGTTA GAAGTGAGTA 1260 GCCCTGTCCC TGGGGGGTGA ATTGAAGCTC ATTCATCTGG AGAAGACTGT TAGTGACAGG 1320 CACTCCTTCC TCCTCCCAGG CCTCCTGAAA TAGGCAGTGT GCTCTTGTAG AACATTACTG 1380 CTTCAACAGT ACACCAGAAA TATTTTAAAG TAATGTTTTA AAATAAAGAA CAAGTCTTCC 1440 ATAACCTTTG TTTTGTTAGT GTTTGTAATC ATGAAACAGA 1480
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