Tag | Content |
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EnhancerAtlas ID | HS095-08225 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr13:31264020-31265480 |
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 | GCCTGCCACG CCCCCATCTA CCTATTAAAC TCCCCCACCT TCCCCAAACC CTAGCAGGCA 60 GACACACATC GGTGGAAGAA GACAGGAGCG GCTGGACATT GAAAGGACGT CGAGAGGAGC 120 ACACCTGCAC ACCATCGACC AGCGGAACGA GGCAGAGTGT GGCTGGAGCA GTCGGAGGGA 180 AGCCTGGGCC GCTGACTCCA GGGGAAAACC ATCTCCTTTC TGGCTCCCCC CTCTGCTGGG 240 AGATACTTTC ACTGAATAAA ACCTTGCACT CATTCTCCAA GCCCACCTGT GATCCGATTC 300 TTCCTGTACA CCAAGGCAAG AACCTGGGAT ACAGAAAGCC CTCTGTCCTT GTGATAAGGT 360 AGAGGGTCTA ACTGAGCTGG TTAACACAAG CTGCCTATAG ACAGCGAAAC TGAAAGAGCA 420 CACAATAGCA CACACTCATT GGGGCTTCAG GAGCTGTAAA TATCCACCCC TAGACGCTGC 480 CATGGGGCGG GAGCCCCACA GCCTGCCCGT CTAGAGGTTT GAGCAGCGGG ACACTGAAGA 540 AGAGAGCCAC ACCCTCATCG CACGTCCTGC GAGGGAGACA AGGGAACTTT TCCGGTTTCA 600 CTTCTGCTTG GCTTGAGCTG GCACTGAAGC ACCCTTTTCC CTCCTCACTG AGGGAGCAGA 660 GGGGAAAAGC GGTAGAACTA ACAGGCTAAC AATGCTCCTC CGAAAATATA TCGTATTTTT 720 GGATCCCTAG AGATAGGTGA TCACGGCAGC CGCGGAGTGC ATTTGGGTCT CCTTTCAAGA 780 AAGAACTTGC TGCTCAGCGT TGAAGAATGC AGTTGGCCAA CAGCCTCCAG CTGCTCTGTC 840 TTCAGCATCT GCCATGGCAT CTGAGCTGAG GTCATGTTCT TCCTGGGAGG TCCCCAGCAG 900 AAGGATCACG TGGAAGCTCC ACAAGCTCCA CAGATGTTCC AGGAGAGGAA TAGGCAGCAT 960 TTGGAAGACA TATCCTGCCA TAACAGAGGG CATTTGCTAG TAGAGACAAC AAACAGCAAC 1020 AGCCAAGTAA ACAAACACAC AAGCACAAAG CACTTTCTCC CATTTCCCCT CATTGATCCT 1080 GTCCGGGTAG AAGCTGGGGA GGAAGTAGAA TAGGGTGAGG CGGGGTGGGG CTGGGGGGCC 1140 TACACCTTCT TCCTTCCCCC GCAGGTCCTG TCCCTGGGCC AGGCTTGAAC TAGGGGAATG 1200 GGAAAAGCTG TGAAGTGAAT GAGAATTAGG AGTTTTTATT TAGACTGGAC TTGAATTTTT 1260 TTTTTTTTTT TTTTTTTTTT GAGACAGAGC CTCGCTCTGT CACCCAGGCT GGAGTCCCGT 1320 GGCGCCATCT TGGCTCACTA CAGCCTCTGC CTCCCGGGTT CAAGCGATCC TCCCACCACA 1380 GTCTCCTGAG TAGCCGGGAT TACAGGTGCC TGCCACCATG CCCAGCTATT TTTTTTTTTT 1440 TTTGTATTTT TAGTAGAGAC 1460
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