Tag | Content |
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EnhancerAtlas ID | HS091-29559 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:241897040-241898490 |
Target genes | Number: 26 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr2:241897541-241897562 | AGAGGAGCGGGAGGAGAGGAA | + | 6.73 |
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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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Enhancer Sequence | TGAGGAGGCG GCTGCTGGAG TGTCGCTTCA CCTCCTCCTG CCTGATGCCA CAACCCGGAC 60 TCCTAGTCCC TTCAAGCAGG GCTGCCCAGA GGAGCTCCTG GCAGCCCAGG GGAGACTTGC 120 CCCTCACTCC ATGAAGCCCC ACCCTGCTCT GTTCCTGCCC CTGAGGCCTG GAGGGTTCCA 180 CGGGGCCCAG GAGGACCAAG CTTGGCATCG GGCCTGTGAC CATGCCCCTC CCTCCTCCCG 240 ACCACTGGCC CAGCAGCTCT CTTGGCTCCA CCCCGTGGGC AGGGACCCAG GAAAGCCCTC 300 CTGGGGCCCT GGGAGCTGAT GCCTCTGGCT CACAGAGGGG CCTTCTCTGG AGCCAGTGCT 360 GGCTTCTGGA GCCTTCTCTT GAGCTGGCCC TGAGTCTCCC CCGGACTCGG TACCAGGCCT 420 GCCAGCCAGC CGGCCTTCCT GGGGAGCTCG TTAAGGGTTC CTTTGCCACC TCGGCTCAGA 480 AAATGGAAAT TAAAACTGTT GAGAGGAGCG GGAGGAGAGG AATGCCGGCC AAGGAGCACC 540 AGGCGCCAGA TGACAGGACA GCGTGCGCCC CTAGGCTGAG TCACCACTGC CATCGGGCTC 600 CCAGCCGATG CCCTGTCCCT GAGGCCCTCA CAGGGGTATC CTGCAGCCAG GCCTCAGGGG 660 CACCCATCAC TGGCAGTGTT GGGGCATGCT GAGGCACAGA GCCATGGCCT AGTCACCCAA 720 GATGGCCCTT CTCAGTCCAG AGAGACCAGA GGGGGTTGTA AAGAATGACG ACAGGAGGCA 780 GCAGCATGGC TCCTTTCCCA AGAGCAGGGG GCACAGGCTG CAGGAACCCC CACCCTAGCA 840 GAATCCAGGT GGACAGGAGG GGCTCCAGAG ATCTGGCACA GGGGCAGCCA TGTGGGCACC 900 TGTGCCCCCA GGAACACAAA GCCAGCTCTG GAGGGAGCCA TCCCCCACCA GCCGCCCCCC 960 GCCAGCCGCC TGCTGCTGCC TGGAGGCTTG GTCCAGTCCC CTGAACCCAG GGGTGCAGAG 1020 CCTGAGCAGG GCAGGGCTCG GACCCTTCAT GTTGAGGACA CTGAGGCCCA GGAAGCTGAG 1080 ACCCCCTGAG CCCCATCTGC CCTGCTGCCG CAACCTGGGC AGGGGTGCAG TGGGGAGGGC 1140 CTTGAGAGGA AGCGGGGTGG TGTCCCGAGG GGCCTGGGGC TTGGGGTGAA GAAGGTGGTA 1200 TTTGTCCATG AACAAGGGGC CATGGGCTGA GCCTGGGGCC TCCTGGCCCG AGGATCCCTG 1260 CTGGCCACAC TGCCCCAAGG CCCGAGAGGA CACCTCGGGT GGTGTGTGCG ACAGGGAGCC 1320 GACTCCAGCT GAGCTCAGTC CCAAATGGAG GGTAGAGCTG CCCAGTGTGT GGTGGTCCCT 1380 GTAGGGATGG GCCCTGCCCC AGGGCGCAGG CTGAGCTGAG GGGCTGCCTC CTGCTGTGTC 1440 CGTGGGCACT 1450
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