Tag | Content |
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EnhancerAtlas ID | HS121-13198 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr16:847090-847690 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr16:847206-847217 | TGGGTGTGGCT | - | 6.14 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH16I000797 | chr16 | 847161 | 847270 |
|
Enhancer Sequence | AGGTGTGGAA TGGGCAGCTG TGGGGGTGGG ACCAGGGTAC ATACCTTTGG GGGTGTGGCT 60 AGGGCAGTCA TGAGGCGGGG CCAAGGCACC CATGGGGTGG GGCCAGGGTA CCTTTGTGGG 120 TGTGGCTAGG GCCCCTCATG AGGCAGGGCC AGGGTACCTT CAGGGCTGTG GCTAGGGCAG 180 TCATGAGGCG GGGCCAGGGT ATCTTTAGGG GTGGGGCCAA GGCACCCATG GGGTGGGGCC 240 AGGGTACCTT TGGGGGTGGG GCTGAGCCAC AGGAGGAGTC TGGCTGAGGG TGGGGCTGGC 300 TCAGTGCCCT AAGGGGGGCT CTGAAGGACC AGCTCCTTAC CCTCAGCATG ACCAGGGTTC 360 TACCCAGGCC TCAGTTTCCC ATCTGGGCAG AAGAGTGGCT GTATTGGCTC TTCTTGATTG 420 GCACCTGGTG GGGAGCAGAT GGCAGTGAGG GGTGAGGGGC AGCTGGCCTG GGCCAGGTTC 480 CGAAAGGTGT CTCAGAGGTG TTCTGGTCCC TCCTCCCTGG GAAGGCTCTC GGTCCTCCTG 540 TCTTGGGTAG GGGCTGGATG GGGCATCTGT CCTATACGAC TGACTAGTCC TTCCTCCCAT 600
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