Tag | Content |
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EnhancerAtlas ID | HS112-04345 |
Organism | Homo sapiens |
Tissue/cell | KELLY |
Coordinate | chr13:80706660-80707960 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Mafb | MA0117.2 | chr13:80707578-80707590 | AGTCAGCATTAT | - | 6.14 | POU2F2 | MA0507.1 | chr13:80707903-80707916 | CTCATTTGCATTT | + | 6.28 |
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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 |
GH13I080130 | chr13 | 80704537 | 80709218 |
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Enhancer Sequence | TTCTATTTCA TTAGAGATGA TATTCACACA CCAAAAATTT GCCAGCTTTC TCTCCTTTTC 60 TTTTTACTTG CTAATTTACT CTAATCTTAC CAGGATTTTT TTTTTTTTTA CTTCTTCTTA 120 ATCTCAATGA GAATTTTACT TTGAAAGAAG GAGCTCTAAC TTTTTTTTTC CTACTCTAAA 180 ACAGTGTTTG TACTTTTTTC TGGACTCCAA GTTGGATGCC TTCACCAAAG TGGTTTCAAA 240 GACTGGAACA AAAAAGCCTC CATCGAGGCC CTGGCTAGCA CAGTCCCTGT TACTTTAAGA 300 GTAGCATTCC ACCTCCCCCT CACACCCACA TACTTGTCCT CTCTTTGCAC AGCAAGTGCC 360 AAGCAGTGAC ATCTACTATA GTTTCTAGGA CACGATGGTC TCTGCTCTAC AGGGAAAAAG 420 AGCGAGCGGG ACAGAAAGAA GGCGGGTGGT GAGGGAGAAG GAGCACAAGC CCAGCTATGT 480 TCCCAGAGGA GGAGTCACTT CCTCGCAATA ATCCTGAGAT GCTGTTTATG GCTGTTCTGC 540 TGATATGAAG CCTGGAGCCG CAGGATGCAG CCTCCCCCTG GCTGTCCATT AATCACGAGG 600 GGCTGTTACA GAGTGTACAG AGTGGGAGTT CTGCCTACAA GTGGCCTCTA ACTGTCTCCA 660 GCTCAATGAA ATGAACCTGT GTGAAAACTT GTTTTATGAG AGATTGGTTT ATTTGTAACT 720 AAACTACTTC CTCTGTTATT TGATAAGATC AAATATTTGC TACTGATAAT CTGAGAGTGT 780 CACATTTATT ATCCTGTTTC AGCCGTTGCC TAACTCCTTT GGAACTGACT CCGTTAACTC 840 TTTGAGGGAC AGCAGTAGGT TTTAGAGGAC CGGTTTCTAT TTTCTTTCAG CAAAGCCAAT 900 GCTATCTTTC AGACACTGAG TCAGCATTAT TTTAGAACAG CTATGACATG TGAATCAAAA 960 AGAAGCCTTT CTCTTCCAAA ACAGAAAGCA GACAACCATA GTAACAGGAG GCTCTGATAA 1020 ATTCCCTGGA GGTTCTGAAG CCACCATGAA AAGGAAGGAA AGGTATTCTG ACTTACTAAT 1080 ATAAAAATGG TTTTGCACGT GCTAGGATTT CTGAAATCAC ACATTTTCAA TATGTTCAGG 1140 ATGACTTTCT ATAGTTTGTT AGACCCTCAA ATATCTATGT GGGGCATGAT CTCTAAATCC 1200 GGCAGCATTC TGCATCTTGA CACTTGGCCT TTTGGAGTCT GAGCTCATTT GCATTTGGCA 1260 GGACTTGATT TCCTGCTTTG ACAGAACGGC GGTAAGGTGG 1300
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