| Tag | Content |
|---|
EnhancerAtlas ID | HS050-01234 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:25429380-25430420 | 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 | TGAAAGACGT GAGTTGAAGG CCACCTCCAC TGCTGGGTGA CCCCAGGCAA GTCACAACCT 60
CTCTGAGCCT CAAATTTTCC AATTCCATGG TCTGTTCATG CCTGGACAGC CTGAGACTCT 120
CTGATCAGGG AGACTTCAGA GCCTACCCCA GAATGCAGGC CCCTCAGACC TAGTGAGGGG 180
GGATGGTGGG CTTCTCCTTC CTCCCCTCTC TATGGTCCCC TCCACTAGTT TCAGGTCCAA 240
ACCCCTCAGG GAAGGGACAG AGGAAGCCAA GACGAATGGG CATCCCCACT CCCCAAGGGC 300
AGGCAGCCCA CATGAGGCCT CTAGGATAAT TACAGCCAGC TGGGCTGCCT CTACCCCCTA 360
CCCCAGCTCC CTGCTCCCTG GAAGCTGGAG AAGCTCAGCA GCTGCCCACA TGTGGTTATT 420
TGAACAGGGA GTGGGAGAGG GAGCTGGCAG GTCCACTGCT GGGCCATGGT GCCAGCTGGG 480
GCCAGCCCTG CCTGACAGCC TTGCTTGAGA ACCCACGTGT ACAGGCAGGG CCAGGAACGC 540
TGAAGTGCTG GGGCTCAGCA ACTTCCCTCC CAGGCTGAGG GGAGCAAGAG GCCACAGGCC 600
TCAGGTCAGA GCCACATGTG GCTGTGGGCT GTTGTCAGCA GATCCCTGCA CAGTGTAAAG 660
CCACGCTGCA AGCTGGGAGT GAGCTGCTGA CAGACGCAGG CCCACATGCC CTGAGGCTGA 720
AAGGCAGGGA TAGGAGCCAG GGCCAGACCC CCGAGGGGAC TCTAGGGAGT TCAGATGGGG 780
CTTCGCCATC AGGCCTGGGA GCCAGAGCCA CGGCCAGCTG CTCTCTGCTC ACGGGGAACG 840
GGACGTCAAG ATGAGCCAGG GTGGTCCCCC TCCCTGCATG AGGGGCTTCT CAATGATGGG 900
GCATGTTGGA TACCATGTTC CCAGCTTACC CCAGTAGAAA CTGCCTTCAG GCAGGGAACC 960
AACCTGGAAG GACTGAGTCA CTGATTCATG CTGGGATGTC AATGACCAAG GGTAGATCTG 1020
AAGAGCTCTA GGTGTGAAGC 1040
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