Tag | Content |
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EnhancerAtlas ID | HS177-21462 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr7:99662960-99664050 |
Target genes | Number: 32 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CEBPA | MA0102.3 | chr7:99663638-99663649 | ATTGCATAATA | + | 6.02 | FOXA1 | MA0148.4 | chr7:99663356-99663372 | GGTTAAGTAAACAATG | + | 7.22 |
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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 |
GH07I100065 | chr7 | 99662784 | 99664116 |
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Enhancer Sequence | CGCTTGAACC CGGGAGGCAG AGGTTGCAGT GAGCCAACAT TGCGCCACTG CACTCCAGCC 60 TGGGTGACAG AACGAGACTC TGTCTCAAAA AAAAAAAAAA TAAAGCGAAT GCTTTCACTA 120 GATAATAACT GCATACCAAG AGCCAGGGGC CATGTTGAAC TGTGCCGGCA CAGCTGTTGT 180 GGATGAGTTT GTGGCAAACA ACCATTATCA GCCACAACTC GTCGGTTTTT TACAGAAGCC 240 ATACAGAAAG AGTGTCTTTT GCGTCTTTGA GGGCAGCAAT AATCACTTCA GTTCCATTCA 300 GGGTGTGGTA TTGTTTCTTG CCACTTTGAT TGGCTGGGGA AGGGCAGGGT GTGCAGGAGT 360 TTCCACTTGA CCCTTCTGCC TATGACCTAA GCTACAGGTT AAGTAAACAA TGTGCTGGGC 420 ATCTGTCCCC CTGCTAAACA TATCCCAATT ATCTTCTCAG GGACATGGCC ATAGGGTGAG 480 TCTGTTCCCA CTGGGCCCAC TGAGATGGAT TTGGGCCAGG ACTCCATTTA TCAGCTGACC 540 TGTGTCTGGA GGGCAATGGT AAGTTTTAGA TCCGTGTCAT ACTAGATCCT GTATCAAAAA 600 GCCTCAAAAG GCCTGGGCAT TCTGTTTTCT TAGTACGTTA CTCTAGTGAA CAGCCACAGG 660 TCCTTTGGGG AAATATTTAT TGCATAATAC TCGTGGTACA GTTGGAAGGT CTTCAAAGAA 720 ACCCAGACTC CCCTTAACTT GATGGATTCC AGATCTCAGA ACTGGCTCAG ATCTGGAAAG 780 CAGCAGCAGG ATTGCAATTT CCCATTGTAA CAGCCGGTAT CAGCCTTCTC ATCAACTCTT 840 GGGATTTTTT GTTTATACAA ATCAAAGCCT TATCCTGTTG GCTGAAAGTT TTTGTTAAGA 900 ACACCAAGGG TTATTAGTCA ATGCCACAGT TCTCTGTGGG TCAAGACACC CTAGTGGGCT 960 GTGCACAGTG GCTCATGCCT ATAATCCCAG CACTTTGGGA GGCTGATGCA GAAGGATCGT 1020 TTGAGCCCAG GAGTTCGAGA CCAGCCTGGG CAACATAGTG AGATCCCATC TCTCTTGTTT 1080 TTTAAATTCA 1090
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