Tag | Content |
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EnhancerAtlas ID | HS185-00849 |
Organism | Homo sapiens |
Tissue/cell | T98G |
Coordinate | chr1:222719800-222720850 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr1:222719935-222719947 | AAATAAACATTC | - | 6.74 | RREB1 | MA0073.1 | chr1:222720358-222720378 | CCCCCAAACACCCTCTTCCT | + | 6.05 |
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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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Enhancer Sequence | GTGTAGGACT GTTTGGCTGA AATTGTTCTT ATTCCTCAAA TCCCTAAAAC AACAGAGCTG 60 CTGACTTTGA CTTTCTGAAA CCTCATGCAA GAGGGAAGGG TCAGGGGTAT AAATTTTTAC 120 CAGGGATGAT CTCAGAAATA AACATTCTCA GTGCTGCTTG TAAAAGCTCA GCTTCTACCC 180 TAATGGGAAT CCTAGAGTTA ATTCTCCAGG AAACAGCTGT GGAGTGGTGT CTAAGAGGAC 240 AGCCCCAGGC GGTGCCACCC AGGTGGCTGA CTTTCTGGGC CAGGCTCAGC TGTAATTCTC 300 TCCTGGACTC TGGGAAGCTC GGTTAACCAC TTCACGCCCT ATGTGGGAGT TACAGTGGTC 360 TGCAGGCTCA GGAACAGTGG CGCCAGGAGT CATGAACAGA TGCCTGTGGA TAGCCAAGTC 420 ATTGTGCTGA CAAGCCCAGG GGGTCTCAGT TCAAAAGGCT GCCTGGACTT CTTGCCTCTC 480 CTCCCCAACA TCATTAGAGG GGTCCTCCCC AGGCAGCCTC TTTTATCAGC TTTCCAAATG 540 CTGACCTCTC CCCATTAACC CCCAAACACC CTCTTCCTAC AAAGTCTGTG TGTGCAGCCT 600 ACACCCGTCT TGTTTTCAGG CTGAGCTCAA TCAAAACGAT GCCTCCCAGG CATGTGGATT 660 TTGGCTGTTG GGCAACCAGG AGAAGCAGAA ACTCTGTGAG TCACTGCTAC TCAGCAGCTT 720 GCATCTCTCT CTTCCAGCTC TGGAGTGCTG GGCAGACAGA ACTCTGGAGA GAGTCTCCAA 780 CCCCTGCCAC CGCCAGGGTG ACGCCAGAGA TGCCCTGGCA CAAATCACCC AGATGAAAAG 840 GACTGGACCC CAGCAGATGC CACCACTCCC TCCCTTAACG CGCTCGGTAA ATTCCACGGG 900 TTTAAGTGCC TAGCTCTCTG AGCACCGCAG AGGATGCAAA TAATTATTTG CCATGCACCA 960 CAGAGGGAGT GTGGCAAATA ATGGCTGCTC TGAGAGCTCC AGGAAGAGTG TCCCTCTCAT 1020 TCTCCTGGAG CCTGGAGAAG AATCAGGGCC 1050
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