Tag | Content |
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EnhancerAtlas ID | HS182-17889 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr5:141442660-141444440 |
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) |
CREB3 | MA0638.1 | chr5:141443719-141443733 | GGGTGACGTGGCAT | - | 6.73 | HNF4G | MA0484.1 | chr5:141442826-141442841 | TGAACTTTGGTCTCT | - | 7.09 | RFX1 | MA0509.2 | chr5:141443594-141443610 | AGTTACCATGGTAACA | + | 7.04 | RFX1 | MA0509.2 | chr5:141443594-141443610 | AGTTACCATGGTAACA | - | 7.05 | RFX2 | MA0600.2 | chr5:141443594-141443610 | AGTTACCATGGTAACA | + | 7.11 | RFX2 | MA0600.2 | chr5:141443594-141443610 | AGTTACCATGGTAACA | - | 7.12 | RFX5 | MA0510.2 | chr5:141443594-141443610 | AGTTACCATGGTAACA | + | 7.28 | RFX5 | MA0510.2 | chr5:141443594-141443610 | AGTTACCATGGTAACA | - | 7.3 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 141443165 | 141444123 | chr5 | 141443042 | 141444398 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I142063 | chr5 | 141442808 | 141444824 |
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Enhancer Sequence | TAAAATTTAA AAATTAAAAG AAAAGAAAAG CTGCTGCAAG GAGAGGAAAG GAAGCTGACG 60 TCTGAGAGGG ATGCAGAGAG AAGAGACGAT AACTGAGTCT TGGTGACTTT CAGGCCTCAG 120 AGCTCCAGCT GCAGCTCTGC CCAGAGCACC CTTTTCCCTA AGCTGCTGAA CTTTGGTCTC 180 TGCCACTTGC ATCCAAAGTG CCCAATGGAC ACCAAGCACC TCCTCCTCAC CCCCTTCATC 240 TGGTGAACCC CTCTGGCTGG AAGTGGGGAG CTTGAGTGAG GACAGAAGCA AGTGTCCATC 300 CCAGAATTGG GGTCCCTCAT TTCTTTCTCT TCACCGTGCT TAACATGATC CAAAATTACA 360 TGTATTTACT TAATTGCTTA CGTGTTTACA TTGATCACCC CTGCACCCCC CAAAAATGTA 420 AAGTTCCATT TTGTCTTGTT TAACTTGGTA TCCCTAGTGC CTGGCACATC ATAGGTGCTC 480 ATGAGTCATT GAATGAACAA ATGAATGTAC AAAGAAGATG GCTTGAAATC AGACCACTGA 540 GACCCCCAAC GAGGTCACAA TTGCAGGAGA AACATCTCAG TGCCAGGCAC TGAGCCTGGG 600 ATGTTTGAAA TTTCTGTGCC CAAGCTGTGT GCCCTTTGGG GCGTGTGTGT ATGCTGGGTA 660 CAAGGCCAGA TACACAATCA ATGCTATAGA AACCACAGAT AAAGGGCCAG GGAGCTGAGT 720 GTGACAATGG GCTGTTGGGA GAAGTTCCAT GCAGATTACA AAGGGTTCAG AAAGGACAGG 780 GGCATTGAAA GGCAGCTGTA ATTAGAAAGC ATAGGCATTC AAAGCTGCCT GGAGGTCAGA 840 GGGGCTGGGC TGGCAGGCTG GGGAGATCGG GCAGGAAATG GGCACGGAAG CCCTGCAGTT 900 CAGGGCTGAC ATAATTGGAC AGAGAGCGGC AGCCAGTTAC CATGGTAACA GCCAATCCGA 960 GTGGCCGCGT ATGTGGCAAG GAGTCAAGGT TTCTAAAGAA GGGGCTAAAA ATGCTGCCTT 1020 TGTTCCCACT TTGAGCGAGT TGCCATCAGA TCCCTGTGGG GGTGACGTGG CATGGGGACA 1080 GAGCCAACAA CTGCTAGCCA CCATGGCTGG GAGGGAGCCA CGTGAGGACC CAGGGGACTG 1140 GCTGGGGCTG GGGAAGCTAA ATATGTCATT CCATGGAGCT GGCTGTGCCT CCCAACATAA 1200 AGCAGCGGCC AATGGCCTGG GATTCAGAGT CTGAGAGTCC AGGGCTCAGA TTGCAGCGTG 1260 GCCTCTTAGC AGCTATGTGA CCTCAGTTTC CTTACATACA AAATGGGACT ACTAACACCT 1320 TTTTCGCAGG GCGGTTGTAA GGATGGAGAG AAGTGATGCA TGTCACACAT TCACTTAGTG 1380 AGTGGTAGAT GCTGTTGTTG TTATTCTGAC AGACAACAAC AGCAGCTCCT CCAAAAGGCT 1440 CTTAGCTTCT GGGGAGTAAA AGGCAGGTTT TGCTTCTTCA GGAGTTTCTT TAGGGGTACC 1500 AAAAAGGCAG TTGATAGAAA CTAAAAAACT CCAGGAGGTG ACCAGCTAGA CTAACCAAGT 1560 GGTATTTAAA AAGAAAACAT TCTTTAGGCA GGCTTGAGAG CTGTGAGATA TCAGAGAATC 1620 CTGCTCCTTT GTTCTTTTGT CCAATTTGTG GGCCTGGACA GGACACAAAG ACAAGGCCAT 1680 CCCTCCCCTC TCCTTCCACA GTGCGGAGAG AAAGCAGAGA AGATCCTGAC ATGAGTGCTT 1740 CCTGAGACTT TTTTTTTTAA TTTTTTTTTT TTTTTTTTTT 1780
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