| Tag | Content |
|---|
EnhancerAtlas ID | HS026-00626 | Organism | Homo sapiens | Tissue/cell | CNCC | Coordinate | chr1:25429270-25430480 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TBX20 | MA0689.1 | chr1:25430408-25430419 | TAGGTGTGAAG | + | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 25429966 | 25430068 | | chr1 | 25430110 | 25430221 |
| Enhancer Sequence | GCACTTGCAT GGGCACTCAG CAGGCACTCA ACTAACAGTT GTTGATTAGA TGAGTAAATT 60
AGGGGCTTGA AAGGGAGACA CGAGGAGAGT CCTAGAAAGG GAGTCAGGGG TGAAAGACGT 120
GAGTTGAAGG CCACCTCCAC TGCTGGGTGA CCCCAGGCAA GTCACAACCT CTCTGAGCCT 180
CAAATTTTCC AATTCCATGG TCTGTTCATG CCTGGACAGC CTGAGACTCT CTGATCAGGG 240
AGACTTCAGA GCCTACCCCA GAATGCAGGC CCCTCAGACC TAGTGAGGGG GGATGGTGGG 300
CTTCTCCTTC CTCCCCTCTC TATGGTCCCC TCCACTAGTT TCAGGTCCAA ACCCCTCAGG 360
GAAGGGACAG AGGAAGCCAA GACGAATGGG CATCCCCACT CCCCAAGGGC AGGCAGCCCA 420
CATGAGGCCT CTAGGATAAT TACAGCCAGC TGGGCTGCCT CTACCCCCTA CCCCAGCTCC 480
CTGCTCCCTG GAAGCTGGAG AAGCTCAGCA GCTGCCCACA TGTGGTTATT TGAACAGGGA 540
GTGGGAGAGG GAGCTGGCAG GTCCACTGCT GGGCCATGGT GCCAGCTGGG GCCAGCCCTG 600
CCTGACAGCC TTGCTTGAGA ACCCACGTGT ACAGGCAGGG CCAGGAACGC TGAAGTGCTG 660
GGGCTCAGCA ACTTCCCTCC CAGGCTGAGG GGAGCAAGAG GCCACAGGCC TCAGGTCAGA 720
GCCACATGTG GCTGTGGGCT GTTGTCAGCA GATCCCTGCA CAGTGTAAAG CCACGCTGCA 780
AGCTGGGAGT GAGCTGCTGA CAGACGCAGG CCCACATGCC CTGAGGCTGA AAGGCAGGGA 840
TAGGAGCCAG GGCCAGACCC CCGAGGGGAC TCTAGGGAGT TCAGATGGGG CTTCGCCATC 900
AGGCCTGGGA GCCAGAGCCA CGGCCAGCTG CTCTCTGCTC ACGGGGAACG GGACGTCAAG 960
ATGAGCCAGG GTGGTCCCCC TCCCTGCATG AGGGGCTTCT CAATGATGGG GCATGTTGGA 1020
TACCATGTTC CCAGCTTACC CCAGTAGAAA CTGCCTTCAG GCAGGGAACC AACCTGGAAG 1080
GACTGAGTCA CTGATTCATG CTGGGATGTC AATGACCAAG GGTAGATCTG AAGAGCTCTA 1140
GGTGTGAAGC TTCTGGGGTT CAGAGCCCTC CAACACATTA TCCTAGGAAA ACCTGGCAGA 1200
AAATGGAATG 1210
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