Tag | Content |
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EnhancerAtlas ID | HS050-56431 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr5:168082760-168084210 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr5:168083107-168083128 | GCCACCTTCCCTCCCTCCTCC | - | 7.22 | ZNF263 | MA0528.1 | chr5:168083113-168083134 | TTCCCTCCCTCCTCCTCCTTT | - | 7.56 | ZNF263 | MA0528.1 | chr5:168083110-168083131 | ACCTTCCCTCCCTCCTCCTCC | - | 7.85 |
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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 |
GH05I168655 | chr5 | 168082216 | 168087238 |
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Enhancer Sequence | ATGGAGTTTC GCTCTTGTTG CCTAGGCTGG CGTGCAGTGG TGTGATCTTG GCTCACTGCA 60 ACCTCCACCT CGTGGGTTCA AGCGATTCTC CTGCCTCAGC CTCCCAAGTA GCTGGGATTA 120 CAGGTATGCA CCACCACACC CAGGTAATTT TGTATTTTTA GTAGATACAG GGTTTCACCA 180 TGTTGGCCAG GCTGGTTTCC AACTCTTGAC CTCAGGTGAT CCACCTGCCT CAGCCTCCCA 240 GAGTGCTGGG ATTACAGGCG TGAGCCACCA CGCCCGGCCA TAAAAATTTA TTTCTTATAA 300 AAAGTTCTTG CCAGCAACTT TTCTGGGGCA TAGGTACATT TTATCAGGCC ACCTTCCCTC 360 CCTCCTCCTC CTTTTTATTT TTCAGATGCT CAGAGTGACA TATCTAGTGA CACAGCAAGT 420 CAGTGGCAGC CCCAGGACTC CATTTCATTT GCTTTTTCTC AAGTGTAGGC GGAGGTAGAG 480 GATATCGGTT ACATTGCAGT GGCCCCTATC AGCTGAAAAG TCCTAATTGT CCACAAAGAT 540 GTATATGGAC TATGCTCCTT ATGGGCTAAG GCCTGCCTAG CCTATGTGAC TCACACCACT 600 GATCTGGGCT GCCCAGACCC ACAACCTCCT CTATTCTTCA GATGCGTATC TGGCAGCCTC 660 TCCTCCACCC ATGGAAAATG TAGAATAGAG ATCATTGTTC TCATAACCAA AGGTGGGGCA 720 GCCTGGCAGA GTGGAAAAGC ATGTGCTTTT AGACTCAGCT GACCCACCCA GCTCTGCAGT 780 TTGCTAGCCG TGGAACTCCA GGCAATGACC CTTTTCTCTA AGATTCAGGT TCTTCATCTG 840 TACTATGGGG GTAACAACCC CTGCCTTGCA GAATTTTTGT GAGGAATGGG GATAAACGTG 900 CAAAAACTCT GGCATGTCCC AGTCACTCTG TAAAAGAGAG CTGTTCCCAT TATTTTCCTC 960 CATAGTTGCG TTGGCTTTAC TCCAATGCTT ACACAAGGTC TGGTTTCAGT CTTCCAATTA 1020 ATTAGCTCGT CAGCTTTCCT TAATCCCATG AGTTCCAGTA TCTTGCACAA GATATCCTGT 1080 ATGTGGGAAA GAGTTCAACA GGCATTCATC AAGGGCTTGT TATGTGCAAA TCATGGTGTT 1140 GTGGTGGAAA GGACATGGCA TTGGGCTTAG TCCAACCTGG TTCAAATCAC ATCTCTGCCA 1200 TCTCCTAGCC ATGTGATTCA GGTCTTTCTC ACTGCTTAAA TGAGGACAAC TGAACCTGCT 1260 GGCAGCTTTG CTTTGGTCTT ACACAAAAGG ATGTGTATAA ATGTGTGATG AAGAGTATGT 1320 GCTCAATGAA TGTCAGATTT TTCATCTCAT TCTGTGAATT CACCTTCTCA CCTGTAACTA 1380 GGCAATCTTC CACTTCTCTA ATCGCTGCTC TTACATCCTA TCATCCACCA TCAAAAGGAC 1440 ATGGGAGATG 1450
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