Tag | Content |
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EnhancerAtlas ID | HS121-38058 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr9:139758320-139760630 |
Target genes | Number: 35 | 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 | chr9:139759295-139759310 | TGAACTCCTGACCTC | - | 6.22 |
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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 | AGCCTAGAAA ATTAGAAAAC ATCAGTGGAT CAAAATTAGC TTTGACAGTA TCCAGCACAC 60 ACCAATTCAG GCCTGCTGTT AGCCAGTTAG CACACTGCTA AGGACTAGTG GTGCCCAAGG 120 ACTGATATGC AGTCCTGGGT TCAGTTACCT AAGCTCAACT AGGCACCATG GCTTATGCCT 180 GTAATCCCAG CACTTTGGGA AACCGAAGTA GCAGGATCAC TTGAGGCCAC GAGTTCGAGA 240 CCAGCCTGGG CAACACAGCA AGATCCTGTC TCTACAAACA ATAAAACACA ACAAAACCCC 300 AAACTCATTA TACAAAAGCC TCTACAATCA GATGTCTAAG AAAGTCACAG TTAACTGCTA 360 AGAGAACACC ACTTCCTTTG CTGTTGAGAA AGACACACTA GGGATTTTTT TTTTTTTTTT 420 TTAGAGTTGA GGTCTTGCTA TGTTGCCCAG GCTGGTCTGG AACTCCTGGG CTCAAGTGAG 480 CCTCTGGCCT CAGCCTCCCT CCTGAATAGC TGGTATGCGT TAGTGGATTC TTTTTGAGAA 540 ATCATATTTA GCACAGATTT ACTTTTCTGC TGGACTCTAC TGCAAAAGTA GGAAGGAACA 600 CCAAATACTG GCCTGGTGTG GCCTTCCTCC CTGAATCTGG TTCCTAGTAA CACAGAGATG 660 ACACATCTCA TGGAAGCCTG CAGGCTCTCC AGAAACATCA CCAATAACAG TGATGCCATC 720 TCATCTACAG TCACTGAATA TTAATATAAT GTATTTATTA ACTTTTTTTT TTTGAGACAG 780 AGTCTCACTC TGTTGCCCAG GCTGGAATGC AGTGACACGA TCTCGGCTCA CTGCAACCTT 840 CGCCCTCCGA GTTCAAGCAA TTCTCCTGCC TCAGCCTCCC GAGTAGCTGG GATTACAGGC 900 TCCTGCCACC GTGCCTGGCT AATTTTTTGT ATTTTTAGTA GAGACGGGGT TTCACCATCT 960 TGGCCAGGCT GGTCTTGAAC TCCTGACCTC ATGATCCACC TGCCTTGGCC TCCCAGAGTG 1020 CTGGGATTAC AGGCGTGAGC CACCGCGCCC GGCCAACATT TCTACCACTT CAGAGGAGTG 1080 ACTTGTGGAG CATCCTAAGT GTGATCTGCT CACAGATGCT GCCACGCAAT TATTCCCATG 1140 ACTCCTAGCT TGTGGCCATT AAGTTTCCTT TAAAAGAAAA GGAGAGTGAA TTTGGTTTTG 1200 ACTGTGCAAC CAGTAAGGGT AGGGCAGACC AATGAATCCC TGTCACCAGA GCCCCAGCGC 1260 ATCCTGGCCC AACTGGCCTC AAAGGCTTCA GCCCTAGGCC ACCTGAGGGT ACGAATGAGG 1320 CAGAGGCGGT GACTAAACTG TCCTCCCTAT TACATCAGAC TCACAACTGA CCCTCGGATC 1380 CATCAGCCAC ATTGGTAATC TCCTTCCACA AGTACTGTTC AGGGCACGCC CATCTTCCAC 1440 CTGTGCAACA GGGTCCACCT GCTCATGGGG TCCCCTGAAG CAGGCACTCT CTACAGCCTG 1500 TGATGCACCC AGGCAGGCTC CCTGGGCAGT ATCTGACCAG CGGAGACCAG TAGAACCAAG 1560 CAGGTCCCAG GCAGAGAGAA AACTCTCAGG GAGGAGCCTA CCCCCTGTCC CCAGCTCCCA 1620 CTCAGGTCAC TAACCTCTGC CCCGTCACCC AGTCTCCCGC CCCAGGCCCT CAACTGCTGT 1680 CCAATGGCCC CCAGCCCTAT CCCAACCCCA ATTCCCCACC TTCATCGCTG GTTCCTGCTG 1740 CTTGCCCCAG TCCCCACCCC TGTCCTAAGC CCTGTACCCC ACTCTACCCT GTTCTTCCAA 1800 GCCCTGTCCC CATCTCCATC CCTGCCCCCG TTCCCAGTGC CCACCCTGGT TCTCTGTCCC 1860 CTATCCTCAC ACAAGGCCCC CAGCCTTGTC CCCGTCCCCG TCCCCACCTC CTGCCTCTGT 1920 CCTCACACCT GTCCCCACCA ACAGTCCCTG CCCCTATCCC CTCCCCGCCC CACCCTGGCA 1980 CTGGTCCCGG CCCTATCGCC TGCCCCTTGC CCCGTCCGGT TCCCTGCTCC TCTCCTCCTC 2040 CAGTCGCCCG CCCCCTGCCT CCTGGGTCCG TCCATCCCCT CCTGGGTCCG CCCCCCACCT 2100 TCCCACCCCT GTCCTGGCCC GGTCCTCCTA CCCCTGCGAT TCGCCCCGCC CTTCGAACCC 2160 CGTCCTGCCC CCGGCACCCC AGCCTTGTCC CCGTCCCCTG CGCCCTGTCC CAGGCCCCGC 2220 CTGCCCTTCC CCGAGCCCCC TGCCCCACGG TCCGTGGCCC CGGCCCAGCG TCCGCCCCGC 2280 CCGGCCCGGC CGCTCCTCAG TCAGCAAAGC 2310
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