Tag | Content |
---|
EnhancerAtlas ID | HS161-06282 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr17:989570-992640 |
Target genes | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF14 | MA0740.1 | chr17:990825-990839 | AAGGGGGCGGGGCC | - | 6.15 | KLF16 | MA0741.1 | chr17:990827-990838 | GGGGGCGGGGC | - | 6.02 | KLF4 | MA0039.3 | chr17:992288-992299 | CCACACCCTGC | + | 6.62 | KLF5 | MA0599.1 | chr17:990828-990838 | GGGGCGGGGC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr17:989959-989974 | TGAACTCCTGACCTC | - | 6.22 | Nr2f6(var.2) | MA0728.1 | chr17:992047-992062 | TGAACTCCTGACCTC | - | 6.22 | RREB1 | MA0073.1 | chr17:990546-990566 | GGGTGGGGGTAGGGGTGGGG | - | 6.27 | SP4 | MA0685.1 | chr17:990778-990795 | AAAGAGGGCGGGGCCTG | - | 6.24 | SP4 | MA0685.1 | chr17:990824-990841 | AAAGGGGGCGGGGCCGG | - | 6.54 | Stat4 | MA0518.1 | chr17:990958-990972 | CTTCCAGGAAAAGG | + | 6.67 | ZNF263 | MA0528.1 | chr17:990285-990306 | GAGGGAGGAGGGAGGGGAGAC | + | 6.79 |
|
| Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
SE_01841 | chr17:990015-991936 | Aorta | SE_23220 | chr17:990087-991720 | Colon_Crypt_1 | SE_23794 | chr17:990282-991706 | Colon_Crypt_2 | SE_24832 | chr17:990194-991785 | Colon_Crypt_3 | SE_26634 | chr17:989867-991898 | Esophagus | SE_26634 | chr17:992160-993023 | Esophagus | SE_28034 | chr17:989906-991951 | Fetal_Intestine | SE_29195 | chr17:990014-992004 | Fetal_Intestine_Large | SE_31579 | chr17:989866-992999 | Gastric | SE_40640 | chr17:989922-991977 | Left_Ventricle | SE_40640 | chr17:992282-995515 | Left_Ventricle | SE_42080 | chr17:990188-991700 | LNCaP | SE_42145 | chr17:989917-991877 | Lung | SE_42145 | chr17:992317-993042 | Lung | SE_49097 | chr17:990322-991723 | Right_Atrium | SE_49495 | chr17:990311-991745 | Right_Ventricle | SE_50313 | chr17:990063-991915 | Sigmoid_Colon | SE_52631 | chr17:990132-991707 | Small_Intestine | SE_54272 | chr17:990363-991768 | Spleen | SE_65254 | chr17:989820-995951 | Pancreatic_islets |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 990609 | 991624 | chr17 | 990720 | 991732 |
|
| Number: 2 | ID | Chromosome | Start | End |
GH17I001086 | chr17 | 990011 | 992101 | GH17I001088 | chr17 | 992161 | 993042 |
|
Enhancer Sequence | ACGGGGGAAG CCGCGCACAC AGCCATGAAC ATGGATGCAC CCGATTTACA CATAGCATTG 60 CTGACAAGCT CCAAAACGAA CATGGGTTGA ACTGTAAAAT ACGATTGCTG ACAAGCTCCA 120 AAACGAACAT GGGTTGAACT GTAAAATATG ATATATGTGT ATACTTATAC ACTTTTTTTT 180 TTTTTTTTGA GATGGAGTCT CGCTCTGTCA ACCAGGCCGG AGTGCACTGG CACGATCTTG 240 GCTCACTGCA AACTCCGCCT CCTGGGTTCA AGTGATTCTC CTGCCTCAGC CTCCTGACTA 300 ACTGGGACTA CAGGCACGCA CCACCACACC CGGCTAGTTT TTGTATTTTT AGTAGAGACA 360 GGGTTTCGTC ATATTGGTCA GGCTGGTCTT GAACTCCTGA CCTCAGGTGA TCCACCCGCC 420 TCCGCCTCCC AAAGTGCTGG GATTACGGGC GTGAGCCACC ACGCCTGGCT TAGACACATT 480 TTTAAAGTAC ATGCAGCTGG GAGCTGTGGT ACACACACCT ATAGCCCTCG CTACTTGGGA 540 GACTGAGGTG GGAGGATCAC TTGAGCCCGA GTTCAAGTCC AGCCTGGACA ACATAGCAAG 600 ACCTTTTTTT TTTTTTAAAG TACAGGCCAA CCCAAAATAG ATACAGATAT GTAGTAAACA 660 CACAAACTGC AGTCTGGAAG GCTATCCACC AAATTCATGC CAGTAGCTGC TTCAAGAGGG 720 AGGAGGGAGG GGAGACTCCA CCTTCATGTG TGACGCTGTA TTTTCTTCAT TAGAAGGTTC 780 TGCTGTTATT CTTTGGAGTT TCTGGTTTAA ATGTTTTTCA ATACAGCAGC AAGGGGGATA 840 CAGCTGCTGC CTGGCTTCCT CAGGGGCCTC TGCTTCCCAC CAAGGTGCTG GGGGAAGTGG 900 GCTGCTGTGG ACCCCCACCC CGGACCACTC TGCTTTCTGC AGGATCCTCA TGCTCCCCAA 960 GGACCCAGAG AGGCTGGGGT GGGGGTAGGG GTGGGGGCAG GCTGGCCGCA GCATCGGCTG 1020 AGCCTGGAGC CTCCCAGTAC AGAGGCAGAG CCCTTTGAGG AAGCTGGTGG GGCAGGGGAG 1080 CGGGGGGCAT CTGGAAAAGC CAGAGGGGAG CGCGAGTGGG GACGCCCGGC GTGACGCCAA 1140 GGCCAGAGGC ATTCAGGTCT CAGCTGCAGA AGGGCAGGAC TTTAAAAGGG GGCAGGGCCG 1200 GACTTTTAAA AGAGGGCGGG GCCTGAGTTT TAAAGGGGGT GGGGCCTGAC CTTAAAAGGG 1260 GGCGGGGCCG GACGGGAGGG AGTTTATTTC CTTTTCCAGG GAGTACTGAG GCCCGGCCCA 1320 TCAATGCCCA CGCTACACGA GGCATACTAG ACAGTCGCTG CCTAAGCCAA AGTCAGATCA 1380 CCGATATTCT TCCAGGAAAA GGCTCCTCTT GCCCCCTTTC CCACAAGAAG GAGAAAGCCT 1440 GGAGGCCCGG GTTGGCACAC CACCCTCCCA GGAGCCAGGG GCAGGAGCCA GCCGTGCGGA 1500 GGCCTGCGTC CAGGGTCACG GTAATCTCAG GGACTGCCGC TGCCACAGTC ACCCCAGGCG 1560 GTAGGGCCCG AGGCCTGGCT TGGCAGGTTC ATTAACTGGG AAGTGCAGGT TGCCTGGAAA 1620 CAGCAGCCTG GCACTGGAGT GATCTCATAA AACAAACAGC AGAGACGCTA ATTCCCTTCT 1680 CTCAGTAACG AATAATCAAA TACCCAGAGT CTTCGGCTGA AAATAAACCA CCTCCGGATG 1740 CCAGACCTGA CCCGGCTCCC CCCGGGCCCT CCCAAATCTG CAGCCCCAGG GGCCTCAGGC 1800 ATCGGTTCAC GATGCTGGGG AGGGAAAGTG GTGGGTAGCA GATTCACGGC CAGGCCTGTG 1860 GAGCCAAGAC CAGAACCGGG GACAGCCAGG TCCAAGTGAC AAAGATAAAC TGTGACAGCG 1920 TTTCCAGCAA CCCTAGGTTT GCTCTCCTCT ACCCTCCTGA GGGATGAGGA GAGGATGCCC 1980 CCCAGGCCAC TCAGCTCAGG TGAGCAGGCA GTGATGACAG GTGTTCACCA TCCCTGAACC 2040 GGAGGGAGCA GGGGGGGGTA TGCTAGAACC AGAGTGTGGC ATTCCCTTGG AAGGATACCT 2100 TCCAGGGTGC CTCTTCCCAA TTTAATAATA ATAATAATAA TAATAATAAT AATAATAATA 2160 ATAATGGCAC TGATGATAAT GACCAGTTAT TGAGTACTTA TTAATTTATG ATGTTCCAGG 2220 CCCTGTTCCA AGCACTTTTT CTTTTACTTT ATTGTATTCT ATTTCTTTTT TTGAGACAGA 2280 GTCTTGCTCT TGTCGCCCAG GCTGGAGTGG AGTGGCACGA TCTCGGCTCA CTACAACCTC 2340 TGCCTCCCGA GTTCAAGCGA TTCTCCCACC TCAGCCTCCC GAGTAGTAGC TGGGATCACA 2400 GGTGCGTGTT ATCATGCCCG GCTAATTTTT GTATTTTTAG TAGAAACGGG GTTTCACCAT 2460 GTTGGCCAAG CTGGTCTTGA ACTCCTGACC TCAGGTGATC CGCCCACCTT GGCCTCCCAA 2520 AGTGTTGCTG GGATTATAAG CGTGAGCCAC TGTGCCCAGC CATTTTTTTT TTTTTTTTTT 2580 TTTGAGACAG AGTCTCAGTC TGTCATCCAG GCTGGAGTGC AATGGTGTGG TTTTGGCTCA 2640 CTGCAACCTC TGCCTCCCAG GTTCAAGCGA TTCTCCCGCC TCAGCCCCCT GAGTAGCTGG 2700 GACTACAGGT GCATTCCACC ACACCCTGCT AATTTTTTTG TATTTTTAGT AGAGATGGGG 2760 TTCCACCATG TAGGCCAGGC TGGTCTCGAA CTCCTGACCT CACGATCCAC CCACCCCGGC 2820 CTCCCAAAGT GCTGGGATTA CAGGCGTGAG CCACCACGCT CAGTCAGGCC TATTCTATTT 2880 CTTTGTAGAG ATAGGGTCTT GCTATGTTGC CCAGGCTGGT CTTGAACTCT AAGCCTCAAG 2940 TGATCTTCCA GCCTCAGCCT CCCAAAGTGC TGGGATTACA GGCGTCAGCC ACCACACTCA 3000 GCCCCATGCA GTTTTCAGAT ATTAACTCCT CAAAATCACC CAATGAGGTA AATACTGTTA 3060 CTATCCTGTT 3070
|