Tag | Content |
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EnhancerAtlas ID | HS157-06890 |
Organism | Homo sapiens |
Tissue/cell | PANC-1 |
Coordinate | chr19:5696770-5699030 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr19:5696782-5696797 | CGGGGTCAGAGGTCA | + | 8.55 | Nr2f6 | MA0677.1 | chr19:5696783-5696797 | GGGGTCAGAGGTCA | + | 7.03 | RREB1 | MA0073.1 | chr19:5698074-5698094 | CCCCCTCACACCCCCCACCC | + | 6.95 | Rxra | MA0512.2 | chr19:5696783-5696797 | GGGGTCAGAGGTCA | + | 6.98 | ZNF263 | MA0528.1 | chr19:5697554-5697575 | GGAGATGGAGAGGGAAGGGGG | + | 6.01 | ZNF263 | MA0528.1 | chr19:5697544-5697565 | GGAAGAGGGAGGAGATGGAGA | + | 6.28 | ZNF263 | MA0528.1 | chr19:5697598-5697619 | GAGGGAGAGAGAGGAGGGGGT | + | 6.33 | ZNF263 | MA0528.1 | chr19:5697502-5697523 | GAGGCAGAGGGAGGAGGGGGG | + | 6.44 | ZNF263 | MA0528.1 | chr19:5698130-5698151 | CCCACCTCCTCCAGCTCCTCC | - | 6.57 | ZNF263 | MA0528.1 | chr19:5697526-5697547 | AGAAGAGGGAGGAGAGGGGGA | + | 6.63 | ZNF263 | MA0528.1 | chr19:5697551-5697572 | GGAGGAGATGGAGAGGGAAGG | + | 6.73 | ZNF263 | MA0528.1 | chr19:5697548-5697569 | GAGGGAGGAGATGGAGAGGGA | + | 6.7 | ZNF263 | MA0528.1 | chr19:5697530-5697551 | GAGGGAGGAGAGGGGGAAGAG | + | 6.92 | ZNF263 | MA0528.1 | chr19:5697541-5697562 | GGGGGAAGAGGGAGGAGATGG | + | 6 | ZNF263 | MA0528.1 | chr19:5697508-5697529 | GAGGGAGGAGGGGGGGAGAGA | + | 7.66 | ZNF263 | MA0528.1 | chr19:5697533-5697554 | GGAGGAGAGGGGGAAGAGGGA | + | 7.71 | ZNF263 | MA0528.1 | chr19:5697586-5697607 | GGAGGAAGAAGAGAGGGAGAG | + | 7.81 | ZNF263 | MA0528.1 | chr19:5697577-5697598 | GAGGGAGGGGGAGGAAGAAGA | + | 8.18 | ZNF263 | MA0528.1 | chr19:5697583-5697604 | GGGGGAGGAAGAAGAGAGGGA | + | 8.18 | ZNF263 | MA0528.1 | chr19:5697511-5697532 | GGAGGAGGGGGGGAGAGAAGA | + | 8.84 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr19 | 5698656 | 5698753 | chr19 | 5697280 | 5698014 | chr19 | 5698092 | 5698417 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I005696 | chr19 | 5696429 | 5697826 |
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Enhancer Sequence | GTGGGTGCAC AGCGGGGTCA GAGGTCACTT GGTAGCCTGG CTCGGCCACA ACGACACCAT 60 GCACCCTCCA GGGCCACAGG GGAGAGGCCA CCTGGAGCCC CACAAGATGT GGCCATGATG 120 TGGGAGGCGG AAATGCTGGC AGCCGCCGGA TGTGTGGCAC CTGCAGGCAC GCTGGTCACT 180 TGCCCTGACT CGCCAGCTCA GATTCTGGGG TCACTGATTC AAAGCCAGAT CTCCCTCAGT 240 CCCATCCCTC AGCTGACACC ATGGTGAAAG CCAGACAGGC GCTGGCAGCA GAAGGCCCCC 300 ACTCCTCACT GAGGGACGCC AGGCACGCCT CAGCCCTCAA GGGCTGGGGT GATACTAGCC 360 ATGGCCAGCA CTGGCTCTCA GGAGGGCTTC CTGCAAGCTC TGTGCTCTGC CCCAGCACAG 420 GGGCCCGGCC CGCGACAGGG ACAGAAGAAT CCCAGGCCCC ACGAGAGACA GTGAGGAAGG 480 CTCTGTCTGT GGGATGAAGA CACAGGGAGG CAGGGATGGA GGGACTGAGA TGCCACTGGG 540 ATGTGTGTGA CACTTTAAGT GTGCAGGGGG GTAAGGAGTG TCTTAGGGAG AGGCCCCGAG 600 CAACGCACGT GAGGAGAGAG CCACGTGAGG GTCTGAGAGA TGTGTTCCAG GCCCAGGACA 660 CAGCCCGTGC AAAGGCCCTG AAACAGGACC ACGCCTGGTG TGTTAGAAGA ACAGTGAGGA 720 GGCCATGAGG CTGAGGCAGA GGGAGGAGGG GGGGAGAGAA GAGGGAGGAG AGGGGGAAGA 780 GGGAGGAGAT GGAGAGGGAA GGGGGTAGAG GGAGGGGGAG GAAGAAGAGA GGGAGAGAGA 840 GGAGGGGGTG GGGCAGGTCA TGCGGGGTCC TGTGGGCTGC AGTGAGAACT TGGGCTTTGA 900 CCGAGGAACG TGGGAGCCCT GGAGAGCTGG GGGCAAAGGA GGGTTTTGCT GCTGTTAATA 960 ACAACGATCC ATCGCCCCGC AGCCAGTCTC CTGTCCTTGT CCTTGTCTCA GGAACCCAGA 1020 GACGTCAGCA GACGCCTGCC CTCCCCGCAG CCCCGCTACC TGGTGACTCC CTCCCAAGGC 1080 CAGAGGTGAC CCAGGCTTGT TCAGAACCCC GCCAGGGTCT CTCCTCCGGC CCGCACCTCC 1140 AGCCATCCCT GAACCAGGCT CCAAGAGGCT TCGCGACCAC TTCAAACCGC TTGCCCAGGA 1200 AGGACTGGGT GCCCCCCACC CCCACCCCTC CACCTTCACC CAGCTGCTCC TTCCTGCTCA 1260 GACCCCAGCC CAACCAAGGG CCTGCAGAAC AGGTCCCCTG TCCTCCCCCT CACACCCCCC 1320 ACCCCCTAGT CAATCTGGGA CTCCCCAAAG CTGCACTGGC CCCACCTCCT CCAGCTCCTC 1380 CCAACTCCCG GCTGGTCAGA GTGGCCGCCC CCTGGGGACT GGACACTGCG CGGGCCAGCA 1440 TGCTGTCACC CTTGCAGCGG GCGGGCAGAT GCTAGGAAGG CCTGAGCCGG GAGGTCGGGA 1500 GCTGGGGATG TTTTTAGAGA AGGCAGAAAT GTTCACTTTA AACCTGGACT CAAGTGAATG 1560 CCTTGCAGGA TGGAAACACG TGGTGGACTC AGCAGATGCC TCACACTCGG CTCTCACTGA 1620 GGCTACGGTT TCCAAAGAAC CGCTGTCTAC AGAGGCTGGC GAGGAGGGAA GCCCCAGAAA 1680 AGCCGCGCCC GGCTGCCCAC CCAAAGGGTC AGGTGGGAGG GCGCTGAACT CTGAGGGCCG 1740 TGGCCCCTGC TTCTGGGCCT GAGGCTGGCC GGGACGAGTG AGCCCACAGA GGCGCCAAGG 1800 TTTCTCTGGT GTGCGCGGCC CGGTCCTCAC TGGAGACCGT CTCTCCTGAC TCCAGCCCAC 1860 AGGCTTCGGG GTGGGGGGTG GAGCCGACCC CACCCCTAGT CCTGGGGCAT CAGCCACAGC 1920 CCACATAGAC CAGCATCTGC ACGGCAAACG CCGGCCCTGC AGCTCTGGCC CGGGCATTGC 1980 AGGTCCTATG CTGGAACTAC CGGGGGTGTC TGCTGAGGGC CGGCCCGAGA AGTCTCTCTC 2040 CCAGGGGTCA AGCCATGGAG GTTCCTGCCA GCGCTGTTTG AGCACCTGGA ATCAGCTGGG 2100 CCTGAAGTCC GCCACATGGC TGGACTTTTC AGTTACTCCA GCATGAGTGG AATCGGTTGC 2160 CCACAACCCG GATTGCTCTA CCAGATGTTA AAGGGTGACC GGAGAAGACG AAGCCCGGCA 2220 GCACAGCTGA GGGGAGTGCG TGGGGAGAGC TGTCAGGCCA 2260
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