Tag | Content |
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EnhancerAtlas ID | HS197-13696 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr21:47329400-47330810 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIA | MA0670.1 | chr21:47330589-47330599 | GGTGCCAAGT | + | 6.02 | RREB1 | MA0073.1 | chr21:47329675-47329695 | ACCCCCCCCACCCACTGCCC | + | 6.14 | RREB1 | MA0073.1 | chr21:47330094-47330114 | ACCCCCCCCACCCACTGCCC | + | 6.14 | RREB1 | MA0073.1 | chr21:47329705-47329725 | CCCCCCCCCACCCACTGCCC | + | 6.66 | RREB1 | MA0073.1 | chr21:47330011-47330031 | CCCCCCCCCACCCACTGCCC | + | 6.66 | SRF | MA0083.3 | chr21:47330135-47330151 | TGCCCAAATATGGGCC | - | 6.04 | SRF | MA0083.3 | chr21:47330135-47330151 | TGCCCAAATATGGGCC | + | 6.26 | Spz1 | MA0111.1 | chr21:47330773-47330784 | GCTGCTACCCT | - | 6.02 | ZNF740 | MA0753.2 | chr21:47329703-47329716 | ACCCCCCCCCCAC | + | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr21 | 47329834 | 47329985 | chr21 | 47330188 | 47330808 |
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Enhancer Sequence | GTAACAGGAC CTTCCCAGCC TGGGCCGCTG CGGAGCCTCT AGGCGGGCTG CGGGTGGTGG 60 CCACAGGCCA GGCAGCCTTC CTGAGCCTTG TCCCTGCTGT CTGCAAGCCC AATGCTGGCC 120 ACGCAGACCC CACAGCTCAA AGTGCGAGAC AGGAACACAG GACCCATGAG CAAGCACAAC 180 TGCACTGCAG GGACCCAGCC CACCCACTGC CCAGATACGG ACCCGGCCAC CCACTGCCCA 240 GATACAGACC TGGCCCACCC ACTGCCCAGA TACGGACCCC CCCCACCCAC TGCCCAGATA 300 CGGACCCCCC CCCCACCCAC TGCCCAGATA CGGACCCGGC CCACCCACTG CCCAGATACG 360 GACCTGGCCA CCCACTGCCC AGATACGGAC CCGGCCACCC ACTGCCCAGA TACAGACCCG 420 GCCCACCCAC TGCCCAGATA TGGACCCCCC CAACCCACTT CCCAGATACG GACCCCCCCA 480 CACACACTTC CCAGATACGG ACCCCCCTCA CCTGCTTCCC AAATATGGAC CTGGCCCACC 540 CACTGCCCAG ATATGGACCC CCCCCACCAC TGCCCAGATA CGGACCCCCC CCACCACTGC 600 CCAGATACGG ACCCCCCCCC ACCCACTGCC CAGATACGGA CCCCCCCCAC CACTGCCCAG 660 ATATGGACCT GGCCCACCCA CTGCCCAGAT ACGGACCCCC CCCACCCACT GCCCAGATAC 720 GGACCCCCCA CCCACTGCCC AAATATGGGC CCTTTCCACC CACTGCTCAC CTATGGATCC 780 TGCCCACCCA CTACACTCCT ATGGGCCGTG CTGGGGACAG GGAGGAACTA GCTGGTCACA 840 TGGTTCTGGG CAAGGGAGGC CCTGGGCACT GGGTGCTGTA TCTACTCCCT GTGAGGGGCC 900 TCCAGGGCAC CTGGAGACAG CCCTGAGCCA TCGGCCTGTC CCAGTGGGCA GAGTTTGCAG 960 ATGTGAACTT CACATCCACA CGTTTGTCCC ATTTCAAGGA AAGCCTGAAT CCTTGCCCTA 1020 TGCAGCAGGG CAGCTGCCCC AATCTTCATT TCCTTTCCCA TGACCAGAGT CCACCTTTCT 1080 CTGTGACCTA AAACTCCACA GAGGAGAGAG GATTCCGTGT ATTTGAAAAG AGTCGTTTGT 1140 CTCCCTGAAA ATGCCTCTGA TTAGATGCCT CCTTGTCTAG CCTTGGCCAG GTGCCAAGTG 1200 CGCCCGAGGG AAGGCACAGG GCCGGGTGCC AGGCCGTGGT AGCAGGGGCA GCATGGGGGC 1260 AGTGCTGGGA TGGCGGTGGG GGAGGGGGCG CGTGGGCTGT ATGCAGGTTT CCAAGGAAGT 1320 GTCCCCCGAG CTGCCTTGGG TGCCGAGACT CGGGAGGTAC TGCTGCCCCA TGCGCTGCTA 1380 CCCTGGTGCT CCCTTCCAAT GTCCCCTCTC 1410
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