Tag | Content |
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EnhancerAtlas ID | HS091-16889 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:28614520-28616900 |
Target genes | Number: 24 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr16:28614663-28614678 | TGAACTCTTGACATC | - | 6.13 | Nr2f6(var.2) | MA0728.1 | chr16:28616245-28616260 | TGAACTCCTGACCTC | - | 6.22 | PHOX2A | MA0713.1 | chr16:28616334-28616345 | TAATTTAATTA | + | 6.62 | PROP1 | MA0715.1 | chr16:28616334-28616345 | TAATTTAATTA | - | 6.32 | PROP1 | MA0715.1 | chr16:28616334-28616345 | TAATTTAATTA | + | 6.62 | Phox2b | MA0681.1 | chr16:28616334-28616345 | TAATTTAATTA | + | 6.62 |
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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 | ACTGCAACCT CTGAGTCTTG GGTTCAAGCG ATTCTCCTGC CTCAGCCTTC TGTGTAGCTG 60 GGATGATAGG GCTCACCACC ACGCCTGGCT AATTTTATAT TTTTAGTAGA GACAGGGTTT 120 CGTCATGTTG GCCAGGCTGG TCTTGAACTC TTGACATCAG GTAATCCACC CCTCTCAGCT 180 TCCCAAAGTG CTGGGATTAC AGGTGTGAGC CACTGCGCAC CGCCTACTTA ATTTATTTTA 240 ACCCAAGAGG ACGAGAACCC AGGTATCACA GAGTGTCCCC AGACAGATTG ACACAACCTG 300 CCAGGAGACA CACCATGAGC TGGCAGTCAT GGCATCAGTG GAAGGCCAAC CCCCAGATGG 360 ACCCCAAGGC CTTGTTCCAG AAGGAGCAGC TCATGTTGGC CCTGTAACCC CAGACCACCT 420 GCTTCTACCG TGCCCTGATC CATGCGCCCC TACAGCGGGT AAAGCAGCCT CCAGGGGAGA 480 GGTCATTGGT GACACCAGGA ACAGGCTGAT CAGAGAAGCT AGGGGTCCTC TTCCTGCTCT 540 GTCCCCCTTG TCCTCATCTC CCGAGCTAAT GGGACCTGCC AGCAGCCCTC CCTCTTCCAC 600 TCCAGCCCCA AAGGCTACCG TCCCCTTGCC AGCCCTGGCA GCCTTGGCAA GCCCCAAGTC 660 AGCGGCTTCC CTTCTGCAGC CCCAGGAGAA CCAGCTCTGA GACAGGAAGC TCCTGCCCTG 720 AACCCACGGC TCCTGCCCCC TCATGCTCCT GGTGACATGG GACACAAGCC ACCTGAGGCC 780 AGGATCCCTG CCTGCCACCA TCTGGGCTGC CCTCGGTCCT CTGAACACAG AGTCCCTGAA 840 AGGCAGCAGA CCCTCTAGCT ATGGCCCCAC TGGGGAAGGA GTCAGCACCT CTTCCTCTCT 900 CCACCTTTTT CACTGCTCTG GGCCTCCAGC CACTGAGAAA AGAGCTCCAT AGCAGCAGGG 960 ACTGGGCCAA GACTTCTTGA CCCCAGAGTG AACAATGGCA GGAGTGGCTG AAAGTCCACG 1020 GCCCAGAGCC TCCTGTGGTC TAGGCTGGGG GAAGGGGGTG CCTGTCATGG CCTGGGGATC 1080 TCTGAGCAGC CCCTCCTGTC TGCCTGCCCC ACAGCCCCAG GATGACTACT TGGTCCTGTT 1140 TGAAGACACT CCTATGCTTG AGTGTCTTCA AGCATTCCCC TCCCCTCGGC GTGGCCCAGA 1200 GGTAGGTGGT GGCTTGTAAG GAGCCCAAGA AAAAGTGACG CTGCCTGGCG GACTCGCCAT 1260 CCACCAACGA CACAGGGCAG GACAGCAAAG GATGTGCTGG GATTAAACAC ATTCCCCCTC 1320 CACTCGTCTC CTGGGTTTTA CTTCTCCAGA CCCTCTCCCC TCTCCAAACA GGTCAAGTTG 1380 AGGAGCTGGA GCGGAGAGGT GGCCGTATTT GGCCCCAGTG GGCGATCACT CTTTCAGCTC 1440 AGGGTTTCTC TTGGCTTGGA ATAGAGACTC TGCATTGAAC ACAAATCATA GTTGTGTTGT 1500 TGTTGTTGTT GTTGTTGTTG TTTTAAGACT GAGTCTTGCT CTGTCGCCCA GACTGGAGTG 1560 CAGTGGTGTG ATCCCGGTTC AATGAAACCT CCACCTCATG GATTCAATCG ATTCTCCCAC 1620 CTCAGCCTCT GGAGTAGCTG GGATTACAGG CGCCCATCAT CATGCCCAGC TAATTTTTGT 1680 ATTTTTAGTA GAGATGGGGT TTTGCCATGC TGGCCAGGCT GGTCTTGAAC TCCTGACCTC 1740 AAGTGATCTG CCAGGCTGAA GTGCTGAGAT TACAGGCATA AGCCACCGAG CCCAGGTCAA 1800 ATAATAACTT AATTTAATTT AATTATTTAT TTATTTTCAA GACAGAGTTT TGCTCTTATG 1860 CCCAGGCTGG AGTGAAGTGG CATGATCTTG GCTCACTGCA ACATCCGTCC CTGGGTTCGA 1920 GCGATTCTCC TGCCTCAGCC TCCAGAGTAG CTGAGGTTAC AGGTGTCTGC CACCATGCCC 1980 GGCTAATTTT TGTATCTTTT TTTTTTTTTA GTAGAGACGG GGTTTCACCA TGTTGGCCAG 2040 ACTGGTCCTG AATCATAATT TATGTTAAGT AAATTGTATT TTATTTATTT CTCAAGCAAG 2100 ATTTGCTCTG TCCCTCAGGC TTGAGTGGAT TAGCCCAGTC AGCCCACTGC AGCCATAACC 2160 TCCCTGGCTC AGGCGATCCT CCTGCCTTCA CTTGTCAAGT AGCTGGGACT ACAGGTGCCC 2220 ACCATCACGT ACAGATAATT TTCTCAAATT TTTGTAGGGA TGATGTCTTG TAATGTTGAA 2280 CAGGCTGGTC CCAAACTCCT GTCCTCCAGT GATCCTCTAG CCTCAACTTC TCAAATTGCT 2340 GGGATTACAG GCATGAGCCA CTCTGCCTGG CCCACAATCA 2380
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