| Tag | Content |
|---|
EnhancerAtlas ID | HS188-10475 | Organism | Homo sapiens | Tissue/cell | Th2 | Coordinate | chr5:138773990-138775090 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr5:138774862-138774873 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr5:138774863-138774873 | GGGGCGGGGC | - | 6.02 | | Myog | MA0500.1 | chr5:138774831-138774842 | GACAGCTGCGG | + | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CGAGACTCCG TCTCAAAAAA AAAAAAAAGA ACATTATGAG ATTTTTTTTT GCAATTTTTT 60
TAAAGTTCAT TAGCTGTCAT CAGTTAGTTA TTTAGTCGTC AGTTAGTGTA TTTTATGTGT 120
GGCCCAAGAC AATTCTTCTT CCAATGTGGT CCAGGGAAGC CAAAAGATTG GATACCCCTG 180
GTTTAAAGGG AGAAGATTCA ATAACAACAC CTGCAGAATG TAAAGAGGGT CATAAGCAAT 240
ACAGTCAAAA GGGGCAGAGC ACTCATGTCT TCTCTGGAGG ACCTGAGAAA GGCTTTAACA 300
ACATCTTTCT TCCGCTTAAC ATCCCTCAGC TACCTCCACC CACTGCTCCT GGACAGTCTT 360
CCTCTAAGTC GGCCTGGCTA ACTCCGACGC ATCCTTCTTG TCACCATTTG TAACACTTTC 420
TGCAAGAAAC CTCCCTTGAC AGCCAGTCTG CGTTAGGTAC CTTGTAAGTG TGCTCTCCAA 480
ATCCCTGACC TTGCTGTGTA GCCCAGGCGT TTTGTATTAT TCGCCCGTTT TGTAATTGGC 540
TGTTCAGTCG TCAAACTCTC TCAGTGGGCT GCGAGTTTTG TGAGCTAAGG GACCCATGTC 600
AGTCAAATCC CCACTGCAGA ATCAGCATTA GGCGGGGCAC ACAATAGGTA TTGGATCAAT 660
ATTTTTTGCC TGACTGTAGG GTGGAAAAGG CTGGTCCTGA TGCCGGCTGG AGCGACATGA 720
TCAAACAGGG ACTGAAGGTC AGGTGGCCCA GTTAGGCGAA AGATAAGGGC CAGGTTAGCA 780
AGCTGCGGAG AGACCGCAGC ACCCCACGGG CCCTCCAGTC ACCTTGGCAT GGGCGGGGCC 840
TGACAGCTGC GGGCCCTGGG CGGGGCACGG GCGGGGGCGG GGCTGGGGGC CGGAGGCAAC 900
AAGTCGTCAC CGGTGACTCT GGGCTCGCGG TCGGTCCCCA GCTTCCCTAC CCCATCCGCA 960
ACCCTACTCA GGCTCAGCAT CTTTTCACAG GCCTCTATCC ATCACCTCAG ACCCAGGATC 1020
TCAGCCCTTG TGCGTCTTCA GGATCCTCAT CCCTGATCTC TCCCGAAGGC CGCCCTATCC 1080
CTCCTTCAGG CGGGGACCTA 1100
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