Tag | Content |
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EnhancerAtlas ID | HS018-06125 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr13:31263660-31265410 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP2 | MA0593.1 | chr13:31265044-31265055 | AAGTAAACAAA | + | 6.62 | IRF1 | MA0050.2 | chr13:31264420-31264441 | ACAGCGAAACTGAAAGAGCAC | - | 6.16 | KLF14 | MA0740.1 | chr13:31264023-31264037 | TGCCACGCCCCCAT | + | 6.72 | KLF16 | MA0741.1 | chr13:31264024-31264035 | GCCACGCCCCC | + | 6.62 | Klf1 | MA0493.1 | chr13:31264564-31264575 | AGCCACACCCT | + | 6.02 | SP3 | MA0746.2 | chr13:31264023-31264036 | TGCCACGCCCCCA | + | 6.41 | SP8 | MA0747.1 | chr13:31264024-31264036 | GCCACGCCCCCA | + | 6.11 |
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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 |
GH13I030689 | chr13 | 31263676 | 31265628 |
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Enhancer Sequence | ACCACACTTT GGGGAAACCA GTTCTGAGAT TCTTCTCCAT TACTCTGACA GGTTGGACCC 60 TCTGGGGAGC AGATCTCAAG ATCAAGTTAT GAGTGCAAGA GGTGTGTTGG GAAGCGATGG 120 TTGTAAAAGA ATCCTGCAGT AGCACCAGGC ACAAGTCTGT CCAGGGAGAG GAGGACTTCT 180 ACTCTCTACC AGCATCTCTC CTAAGTCCCC TTAGGGGACG GGGGCAAGGA AGTGCTGGGA 240 AGGGCAGGGC ATGGTTCCTG GCTAGGACTC CACCCCCCTG GGGCCTGTAC CCACGGACCT 300 AGGTGAAGAC AGGCACTCCT GCCTTCTCGC CCAACGGTTG CGTTTCCCAA GATCATCCTG 360 GCCTGCCACG CCCCCATCTA CCTATTAAAC TCCCCCACCT TCCCCAAACC CTAGCAGGCA 420 GACACACATC GGTGGAAGAA GACAGGAGCG GCTGGACATT GAAAGGACGT CGAGAGGAGC 480 ACACCTGCAC ACCATCGACC AGCGGAACGA GGCAGAGTGT GGCTGGAGCA GTCGGAGGGA 540 AGCCTGGGCC GCTGACTCCA GGGGAAAACC ATCTCCTTTC TGGCTCCCCC CTCTGCTGGG 600 AGATACTTTC ACTGAATAAA ACCTTGCACT CATTCTCCAA GCCCACCTGT GATCCGATTC 660 TTCCTGTACA CCAAGGCAAG AACCTGGGAT ACAGAAAGCC CTCTGTCCTT GTGATAAGGT 720 AGAGGGTCTA ACTGAGCTGG TTAACACAAG CTGCCTATAG ACAGCGAAAC TGAAAGAGCA 780 CACAATAGCA CACACTCATT GGGGCTTCAG GAGCTGTAAA TATCCACCCC TAGACGCTGC 840 CATGGGGCGG GAGCCCCACA GCCTGCCCGT CTAGAGGTTT GAGCAGCGGG ACACTGAAGA 900 AGAGAGCCAC ACCCTCATCG CACGTCCTGC GAGGGAGACA AGGGAACTTT TCCGGTTTCA 960 CTTCTGCTTG GCTTGAGCTG GCACTGAAGC ACCCTTTTCC CTCCTCACTG AGGGAGCAGA 1020 GGGGAAAAGC GGTAGAACTA ACAGGCTAAC AATGCTCCTC CGAAAATATA TCGTATTTTT 1080 GGATCCCTAG AGATAGGTGA TCACGGCAGC CGCGGAGTGC ATTTGGGTCT CCTTTCAAGA 1140 AAGAACTTGC TGCTCAGCGT TGAAGAATGC AGTTGGCCAA CAGCCTCCAG CTGCTCTGTC 1200 TTCAGCATCT GCCATGGCAT CTGAGCTGAG GTCATGTTCT TCCTGGGAGG TCCCCAGCAG 1260 AAGGATCACG TGGAAGCTCC ACAAGCTCCA CAGATGTTCC AGGAGAGGAA TAGGCAGCAT 1320 TTGGAAGACA TATCCTGCCA TAACAGAGGG CATTTGCTAG TAGAGACAAC AAACAGCAAC 1380 AGCCAAGTAA ACAAACACAC AAGCACAAAG CACTTTCTCC CATTTCCCCT CATTGATCCT 1440 GTCCGGGTAG AAGCTGGGGA GGAAGTAGAA TAGGGTGAGG CGGGGTGGGG CTGGGGGGCC 1500 TACACCTTCT TCCTTCCCCC GCAGGTCCTG TCCCTGGGCC AGGCTTGAAC TAGGGGAATG 1560 GGAAAAGCTG TGAAGTGAAT GAGAATTAGG AGTTTTTATT TAGACTGGAC TTGAATTTTT 1620 TTTTTTTTTT TTTTTTTTTT GAGACAGAGC CTCGCTCTGT CACCCAGGCT GGAGTCCCGT 1680 GGCGCCATCT TGGCTCACTA CAGCCTCTGC CTCCCGGGTT CAAGCGATCC TCCCACCACA 1740 GTCTCCTGAG 1750
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