Tag | Content |
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EnhancerAtlas ID | HS026-02896 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr1:206698980-206700020 |
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) |
RREB1 | MA0073.1 | chr1:206699634-206699654 | GGGCTGGGGTTGTGTGGAGG | - | 6 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_27159 | chr1:206698011-206699785 | Esophagus | SE_32205 | chr1:206699025-206700363 | Gastric |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I206524 | chr1 | 206698069 | 206699625 |
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Enhancer Sequence | TGTTATGTTG CCCAGGCTGG TCCCAAATTT CTGGCCTCAA GCAATCCTCC TGCCTCAGCC 60 TCCCACAGTG CTGGGATTAC AGGCGTGAGC TACCTTGAGG GCCCCAGAGA GAATTTTAAT 120 ATCTACTTTG GTGTCTGAGC AACAACTGAG CAGATCTTAT GCCTTTCCCT TTAGTACAAA 180 ATGGTCGCTA AAAGTGTATG TCAATCCCAT CCAGCCCTGC CACACAGAAA ACTGATACAG 240 TCATTTTGGA AGAGAGTAAA GACCAGGATC TTGGGGTGGT CTTTGGCTCT CTTTCCTGTG 300 CCTCAGTTCA GCAGAGGCTC CCAGCTTCAC CCCACCTGTC CAGCACTTTC CCTTCTCACC 360 GGCCTTGGAG GAACCTGCTT CCATAAAGCC CTCCACCCCA ACCCACTCTT TTACATGGGA 420 ACTCAGCATC TGAACCAAAC TGGAGCTTGC TCAGGTGCAT CCCCTCTTGG CTGTTCTCAC 480 AGAGACGACA GCCCCTGTGT GTCAGCTGCC CATCTTGCCT GTCCACATGA GGGGCTGGCC 540 ATCTCTGACC TTAGAGTTGC AGGACACTCG TCTTACCATT ACATTGACCT TTCCTGTTTG 600 CTTCCTGGCT TGCTTTCTGG CAGTGTGTGT GTGTGTGTGT GTGTGTTGGA GTTGGGGCTG 660 GGGTTGTGTG GAGGGAGGGA GCAGTTGTGT GCCTCCAGGC CCTCCGGGCT GGGCTGCAGG 720 ATGCTGAATG CCCCCAGGGT GGTCTGTCCT CTAAATCAAG GAACTACAGT AAGTGGTCTC 780 AAGAGGGCTG AGCTTTGCCT CCTTCCTGGA AACATAAGGA TGCAGATGTC CTGACCTGGC 840 TGCCTGACCC TTGGAGTGGG GAGTTTCCAT TCCCTTGCTG CCAGCCTCAC TAGGAGTTTA 900 GCCAGGAGTT TGAAAAACTT ATAGATCATG TTGATTTTGG CAATGGCTGC AGACCTCCAG 960 GCTTGACTAT CACAGTCTCT CCGCCTTCCC ATTCACCAAC ATGACCTATC CTTCCAGCCC 1020 CCCTGCCTTA CTCCTCTGCA 1040
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