| Tag | Content |
|---|
EnhancerAtlas ID | HS050-01808 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:39043520-39044730 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:39043820-39043841 | TGTTGAGGGAGAGGAGGAGGG | + | 6.16 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGAATTTTTA GCCAGCTTTA GAACAGTGTT GGAGAGCTGT GCTTTGGAGA AGGGGACCCA 60
GTGGCAAAAG AGGCAGTGCC CAGAGTTAAC GTCATTGGGA TGGTCAGCCA GCAAAAGCCA 120
CATGGATAAT GGGGACTTGG CCCACATAGG ACCTGAGGCC CCTTCCCTTC TATTCTCCTA 180
GATCTACAAG AACCCTCTGA AAGGATCTGA AAAGTACATG GGACCAAGGC TTTTCTCCAA 240
ACCACCATGC AGGCATCAAC CACAGGAATG AGAGGCCTGA GCTGAGACCG GCATCCTTAC 300
TGTTGAGGGA GAGGAGGAGG GAGAGACCGG AGGCAAAATT AGAGAGGACC CAGCCAGGAT 360
GGAGAAAGTG AGATTGGGAG AATGAGACAA ACGGAAGTAA AGACAGAGAC CGGGAGAGAG 420
AGGCAGAGAG CTGGACCTGG GAGAGATACA GATGGAGAGA GGCGGAGATG GAAGGAGCCG 480
AAGGGACCAG AGAGAGCGTG GACGGGAGGA AGACAGACAC GAAGAACTTA AGAGGGGAGC 540
GCGCCCAGGA TGGGAGCGAG CCAGAGAGGA GGGGGCGGCG GCGGCGAGAG CGGGCGGGGG 600
ACACGGGGAC CGGGAGACGC GATCCGGAGA GCGGTGGGAA GTATTCGCCT CCGTTCCTCA 660
AACACAGGAT GCGAGCGCCC TTTGGAGAAG TCGCGCTCGG CGGAAACGCT AACTCCCCGG 720
CCAAGTGCAA ATGTAAAGAG GCCCTGAGAG CACTTTGTGC AAATATCAGG CCGGGAAGTG 780
CTGCGCCCGC GGAGCTGCCG GGCACCTCGG CGCCCCCGCG CCCTCGGCTG CGCGCTAATT 840
CACTTTGCCG TCACCTCTCG GGCGGGGTCG GGCGGGCGCG GGCAGCCGGA GCGCGCAGAG 900
GGCGCAGAGC GCCTCGCAGG GCCAGGGGCC GCGGCCCTGC CTAATGGAGC AAAAGACAGA 960
TCAGCAGAAG CAAGGCAGGT GGGGCGGGAG CGGGAGCGTG GACATCCGGC ACGAAGTCAG 1020
AGAAGAAGCC GCAGAGACTC GGAGGAGAGA GCGCTGGGCT GCTCAGGACC TGGCCTCGAG 1080
TTTGGGGCTT CCAGGTTGTC AGGAATGGAG ACTCTCAGCA AGACCTCCAC AGCCTCCGTT 1140
TACTCCTCTA TAAAATAGGA AAATAAAGCC TTTCCTGTTC ACCTCAGGGG GCTTTTGTGA 1200
GGCTGGAATG 1210
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