Tag | Content |
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EnhancerAtlas ID | HS048-02115 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:116253460-116254340 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr1:116254263-116254275 | GTTTGTTTGTTT | + | 6.32 | SOX10 | MA0442.2 | chr1:116254275-116254286 | TGCTTTGTTTT | - | 6.02 | ZNF263 | MA0528.1 | chr1:116254169-116254190 | TCCTTTCTCTCCTCCACCCCC | - | 6.07 | ZNF263 | MA0528.1 | chr1:116254014-116254035 | TCCCCTTTCATCTCCTCCTCT | - | 6.83 | ZNF263 | MA0528.1 | chr1:116254163-116254184 | TCTTCTTCCTTTCTCTCCTCC | - | 7.41 | ZNF263 | MA0528.1 | chr1:116254166-116254187 | TCTTCCTTTCTCTCCTCCACC | - | 7.4 |
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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 |
GH01I115713 | chr1 | 116253961 | 116254110 |
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Enhancer Sequence | ACCAGGAGGT TTCCCACGGC AAGCGACTGG CCTCTGGGAA TCACATCTTT GTGGGAGGAG 60 AAACTGGTGA TTATCCTCTT CTGTTTCCCT GGCAGGGACT GGTGGGAATG AGCCTTCACC 120 AAGCCCTAGG GGACCGGTCC CAGGCCAGGC ACAGCCAAGT CAGGAGCCAA GGCCACATTC 180 GGCAGAGGCT CATGTGTCTC AGACCAAGCA GTGGTCCAGG AGTGAACAGG TCCACAGCAT 240 GCAGCCTGCC CTGCCCTGCT ATCTGTCCTC ATGGCCCCAC TCCTGGGGGA GCTGGCTGTG 300 CTCACTCCAC AAAGGCACGG AAAGGGACCC TTCCTGACTC CATGCCATGG GAAGTTCTGG 360 GCCTCAGGGT CTCTGCTCCT GTGAGGAGAG GCCTGAGCTT GGGAGGGCCA AGCTCTTAAA 420 GTGGGGTCCT GCCCTTGCTT GTGTGGCAGG TGGACAGATA AACGGCCGGG GCTGGAACCA 480 CACAGCTTAG AGGTTGTGTC TAAAGAGGGC ACTGGGTCTG GAGTTTAAAG ACCTTGCACA 540 GGTTGCTTAA CCGCTCCCCT TTCATCTCCT CCTCTGAAAG TGGAGAGAAC AGCTGCCACA 600 TGACTTCTCA GGCATGTTGA TATAACGAGA TGCTATCAGC ATGTGGGTTG GGCAAAGTGT 660 GTAGGGAGAC ACATGCAGAA GGTCCTCATA AAGACTTTGT CTGTCTTCTT CCTTTCTCTC 720 CTCCACCCCC ATCAAACTCT TACTCATTTT AAGATTTTTT TTTTTTTCAC TACTTTGATC 780 CTTCGTTGAT GGGAAGGGTT TTTGTTTGTT TGTTTTGCTT TGTTTTTGTT TTTGAGATGG 840 AGTCTCACTC TGTCACCGAG GCTGGAGTGC AATGGTGTGG 880
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