Tag | Content |
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EnhancerAtlas ID | HS182-00010 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr1:1502260-1503740 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
YY1 | MA0095.2 | chr1:1502433-1502445 | CAACATGGCTGC | + | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I001566 | chr1 | 1502143 | 1504276 |
| Enhancer Sequence | TGAATGAGTA ACAGTGTCAC AAGAGAGGAA AAACTCAGGC AGAGGGGGCT GCTGGAGTGT 60 AACCAGTCTC TATGCGGATA ATGGGGCAAC ACCCAGCAAG TGAAAACTAC CTGTGCCTTT 120 CTCACAGACA CTGGCTTCTA GAAACCCGCC CTACGGACAT ACACGTGCCT CTGCAACATG 180 GCTGCCTGCA GGATGCCCAC TGCCGGCCTT CCACAGCCAC AAAAGAACAG ACAAGTAGAA 240 TAATCCATCC ATGGGGCAGG ACAGGCCATG CGGCTCCACG CGCACCTCCG AAGATGAGTA 300 GAGGAAGCAA AAGAGCCCAA GGGCACCCTG CTGCGCCACC ACACACGTCA CCCACACACA 360 CAGAGAAGAT GTGCTCATCT AGTGTACGTG AAACACCTGA GTCCCCTGAG GCTGATGACA 420 GCTGCGTCAG TCCTTACATC CCTAGATATT CCGAGCTACA CAACCCGGCT CTCCAAACAT 480 CTACCACACA CGGCCAGAAA TGTGGCACAA TAGCAGCGAT TCATGACTAC AAACCCGTGT 540 TCACGGCACC CGGACTGTGA AATAAACGTG AAAATGCTAA AATTAAAATT CCTGACATTC 600 AGTCATAACC ACAGATCCTG ACGGAAACAT GAGGTTAAAG CAATAAAGTC AACTGTTGGT 660 TGTGACTGAG AGGGTGACGG AGGCCCAGAC ACAAGGCATA CCACAGGGAG CACACGTGAG 720 AAACAACAAG CCTAAAATGA CTTCCTTACC AATTCAGACA ACATACAATA AAATATGTTC 780 CGTCAAAGCA CAAACAAGGG CCGGACGCGG TGGCTCACTT GAGGTCAGGA GTTCGACAAC 840 AGCCTGGCCA ACATGGTGAA ACCCTATCTC TACTAAAAAT ACAAAAATTA GTCATGGTGG 900 CACACGCCTG TAATCCCAGC TATTCGGGAG GCTGAGGCAG GAGAATTGCG TGAACCCCGG 960 AAGCGGAGGT TGCAGTGAGC CGAGATCGCG CCATTGCACT CCAGCCTGGG AAACAGAGCG 1020 ATACTCTGTT TCAAAAAAAA AAAAAAAAAT CGCACAAAGA AGCCCAGGAT CAGCGTGATC 1080 ACAGCAGCCA AAGGAGACAG CCTGCCTCCC AACACCAACA AGAACTCACC ACCTGCTGGA 1140 CGTTCCTTTA AGTTAGCCTA TTTAAAAACA AAATGCAGTT TGTTTTTCCC CCAACAAAAG 1200 GTTCACGAAT GGCAAAAAGG CTATTTAGCA ACAGAAGCAG TATTTCTCCC AAACTGATGC 1260 AACCGACAGG GCAGCCAGCT TGCGACTCAA CAGCGTTTCT TACATAAAAG CAAGGACAGC 1320 TTGGAAAACA CTCCTGACAC CAACAGGCTT CGCCTGAAGG GCCAACGCCT TTGTAAACTA 1380 ATCTTCCAGA CAAGTATTTG TCTGGTATGC CAAACAACTG TCTTTACAAG TACCAAAAAT 1440 CTATCAGAGG GCTTGTAATC CCAGCACTTT GGGAGACCAA 1480
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