| Tag | Content |
|---|
EnhancerAtlas ID | HS120-02574 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr17:990160-991790 |
Target genes | | Number: 15 | 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 | | KLF5 | MA0599.1 | chr17:990828-990838 | GGGGCGGGGC | - | 6.02 | | 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: 17 | 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_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_42080 | chr17:990188-991700 | LNCaP | | SE_42145 | chr17:989917-991877 | 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: 1 | ID | Chromosome | Start | End |
| GH17I001086 | chr17 | 990011 | 992101 |
|
Enhancer Sequence | ACATAGCAAG ACCTTTTTTT TTTTTTAAAG TACAGGCCAA CCCAAAATAG ATACAGATAT 60
GTAGTAAACA CACAAACTGC AGTCTGGAAG GCTATCCACC AAATTCATGC CAGTAGCTGC 120
TTCAAGAGGG AGGAGGGAGG GGAGACTCCA CCTTCATGTG TGACGCTGTA TTTTCTTCAT 180
TAGAAGGTTC TGCTGTTATT CTTTGGAGTT TCTGGTTTAA ATGTTTTTCA ATACAGCAGC 240
AAGGGGGATA CAGCTGCTGC CTGGCTTCCT CAGGGGCCTC TGCTTCCCAC CAAGGTGCTG 300
GGGGAAGTGG GCTGCTGTGG ACCCCCACCC CGGACCACTC TGCTTTCTGC AGGATCCTCA 360
TGCTCCCCAA GGACCCAGAG AGGCTGGGGT GGGGGTAGGG GTGGGGGCAG GCTGGCCGCA 420
GCATCGGCTG AGCCTGGAGC CTCCCAGTAC AGAGGCAGAG CCCTTTGAGG AAGCTGGTGG 480
GGCAGGGGAG CGGGGGGCAT CTGGAAAAGC CAGAGGGGAG CGCGAGTGGG GACGCCCGGC 540
GTGACGCCAA GGCCAGAGGC ATTCAGGTCT CAGCTGCAGA AGGGCAGGAC TTTAAAAGGG 600
GGCAGGGCCG GACTTTTAAA AGAGGGCGGG GCCTGAGTTT TAAAGGGGGT GGGGCCTGAC 660
CTTAAAAGGG GGCGGGGCCG GACGGGAGGG AGTTTATTTC CTTTTCCAGG GAGTACTGAG 720
GCCCGGCCCA TCAATGCCCA CGCTACACGA GGCATACTAG ACAGTCGCTG CCTAAGCCAA 780
AGTCAGATCA CCGATATTCT TCCAGGAAAA GGCTCCTCTT GCCCCCTTTC CCACAAGAAG 840
GAGAAAGCCT GGAGGCCCGG GTTGGCACAC CACCCTCCCA GGAGCCAGGG GCAGGAGCCA 900
GCCGTGCGGA GGCCTGCGTC CAGGGTCACG GTAATCTCAG GGACTGCCGC TGCCACAGTC 960
ACCCCAGGCG GTAGGGCCCG AGGCCTGGCT TGGCAGGTTC ATTAACTGGG AAGTGCAGGT 1020
TGCCTGGAAA CAGCAGCCTG GCACTGGAGT GATCTCATAA AACAAACAGC AGAGACGCTA 1080
ATTCCCTTCT CTCAGTAACG AATAATCAAA TACCCAGAGT CTTCGGCTGA AAATAAACCA 1140
CCTCCGGATG CCAGACCTGA CCCGGCTCCC CCCGGGCCCT CCCAAATCTG CAGCCCCAGG 1200
GGCCTCAGGC ATCGGTTCAC GATGCTGGGG AGGGAAAGTG GTGGGTAGCA GATTCACGGC 1260
CAGGCCTGTG GAGCCAAGAC CAGAACCGGG GACAGCCAGG TCCAAGTGAC AAAGATAAAC 1320
TGTGACAGCG TTTCCAGCAA CCCTAGGTTT GCTCTCCTCT ACCCTCCTGA GGGATGAGGA 1380
GAGGATGCCC CCCAGGCCAC TCAGCTCAGG TGAGCAGGCA GTGATGACAG GTGTTCACCA 1440
TCCCTGAACC GGAGGGAGCA GGGGGGGGTA TGCTAGAACC AGAGTGTGGC ATTCCCTTGG 1500
AAGGATACCT TCCAGGGTGC CTCTTCCCAA TTTAATAATA ATAATAATAA TAATAATAAT 1560
AATAATAATA ATAATGGCAC TGATGATAAT GACCAGTTAT TGAGTACTTA TTAATTTATG 1620
ATGTTCCAGG 1630
|
