Tag | Content |
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EnhancerAtlas ID | HS030-02630 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr10:830480-832170 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr10:830865-830876 | CTGAGTCATCC | - | 6.32 | JUNB | MA0490.1 | chr10:830865-830876 | CTGAGTCATCC | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr10 | 830904 | 831008 | chr10 | 831955 | 832079 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I000783 | chr10 | 829643 | 831697 |
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Enhancer Sequence | GGCAGGATTT GCAATGCCTC CTGCAGGCGA CAAACTGTCT CCCAAGGCCA GACGCAGACA 60 GAGCTGTCAC CGCTCCCACG CCCGGCGTTC CGGGAGCCTC CCTCCCATCC CCAGCAGCAG 120 ACGCCACCTG CCCCCCACCT CCCGCCCCGG GGTCTGAACT CCCAGCCAAG CCCGGCCTCT 180 GCACACAGCA GTGAGAAGCC AGGACCTACG CACACCCCTG GCCGGCTCCC CGCTGGCCCC 240 TCTGCGCGTG GGAGCTTCCA GCCTCCCGGG TCTAGGGGAC TGGGGGATGC GTCTTCCTCC 300 CGCCCCCGCA GCGCCCGGGG CAGGAGTGGC ATCGGCGTCC CCGGCGTCCC CGCATCGGGC 360 TTCTCTGGTC CTTTGTGAAT CGGGCCTGAG TCATCCCCGG CTCACGGCTG CGCCACGTAC 420 CCACTGGGCG CTTTCCTCCG AGCGCTGACG ACAGCGACTC CACCGGCAGC TGCTTCCCAG 480 CGTCTCACGG CGGGCCCTTG GCTCCCCTCT CTGCTGTTTA ATCCGCTGAG GAGCCCTGGT 540 GAGCACGAGA GGGGCTCGTG GCTGATCAAT GCGGGCCGAG GCTGCTGGCA CCTTTCTCCA 600 GGAAACACAC CTGGCGTCCT GCAGGGGCCG GACCGGAGAA GCCCTGTGTG CCCCATACAG 660 CGTGTGCTGC GGGGCAGCCT TTGTGCCCTC GAAGCCGGCC AGGGCCTCCG AGGACTGTTC 720 CAGGAAGGCT CCAGAGAGCA ACGTCCCCAG TTCACTCACA GCTGGCCGCC CCCAGCCCCC 780 TGCCCGCAGC ACCCGCCGTG TCTCCTGCTG GGAAGAGTGG CTGCTGTAGC TTCCTCCCCC 840 TGCCCCTCCT GCCCGCTCTC CTGCCCCATC AGCATCTCAG GGCCGCATGG AAAGCTGCGG 900 GGTGTCAGCA CAGGCCAGGG TGGGCTGTGG AACAGACACC CCAAGGCAGG GCGTTGGCAG 960 GCGAAAGCTC CTGCCTCCCT GGCGTGCTGG CTGGAGGGGT CCATCGGCCC CCAGGACACT 1020 GCCCTCCTTC ATGTCCCCGC GCAGCCCTGG GAGGAGCCTG GAGGGTCAGT GCCGACTCTG 1080 ACGTGCCCCC ACAGGTGACA GTCATTTCTG CCCAATTTTA TTGTTCAAAG CAAGATGCCT 1140 GTGGCAGCTG CCTGAGCACG TGGGGTCTCC GGCCCAGAGG TGCTCCTTAC CAGTGTGCAA 1200 GTGAGAGGGG GGACTGATAA ATAAATGGGA GGCGGAGTAG GCTGATGGGG GTGAGGGGTC 1260 TCACCACAGA GAACACACTG GGAGTAGGAT CCGAACCTCG AGACCAGCTT TGAGTGTCTA 1320 GGGAAGTCCT CGTGGGGGGG TATTTACTTT ACAGCGAACC ACAAATGTTA AGCTACAAAG 1380 TGGCCTAGAG GTAAGGAGGA CCCTGAAGGC CAGTCCCCAG ATTTCAATGC ATGGCGTCCT 1440 GCAGGATGGA GCCGGGCGGG GCTGGCCGGC CAGGGGAGAA GCTCCAGGGT CCAGGGGCAC 1500 CTTATCTCTA AGGTCAGGAC AGGACCGAGG GAGGGCTGGG GAGAGCACCT GGGCGGACGA 1560 GGCCTCCAGC CGCACACAGA CAGGGGAGGG CGAGGGCTCT AAGCAGGGCG TTATGGCCGA 1620 CACAAGGCGG CCTTCGAGGA GCTTTCCCAA CTGAATTGCA GCTGGAGCCC CTCCAAGAAG 1680 AAGTTTCAGC 1690
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