| Tag | Content |
|---|
EnhancerAtlas ID | HS121-11616 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr14:105611400-105612060 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr14:105611618-105611637 | CAGCTCCACCTGCAGGCCA | - | 6.42 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGGCAGAGAC AGGCAGTGCG TGGGCAGGGC AGGGCCGTGA ACCTGACACC TACATCCCTG 60
GACTGGCGCT GTGGGTACAC GTGGGACACA CCCTACAGCC CGCCCAGGAG AGCACAGCAA 120
GGATGCCAAG GGCCTGGGGG GGCAGCTTCC CACCCGGCTG TGCCCTATAC CAGGAGGCAG 180
GAGTGACGGT GCCCACCCGC CCATCCTCAG GGCGGACCCA GCTCCACCTG CAGGCCAGTG 240
GGGGAAGGAG AGGCAGGGCG GGGTACAGTG GGTCTCCTCC AGTTCTGAGC CCCTCCTGGG 300
AGACAGGGGC CCAGCTCCAA GCACACAGCA GGCAAAGGTG GCTCCTAGGC CAGGGCAAAA 360
CTGCCCACGG AGCTACAGCC CAAGAGCTGG GGCCAGGCAG CCATGGCGCC GTCAGTCCAG 420
GCCCTCAGGG CAGCTGGACA AACAGGCACC CCCAGCTGGC TGCTCTCCCA GCCTCCTCTG 480
CCACCTCCAC CCAGCACCAG GCCCAATGCC CCTCTCATCT GACCCCACAG GGCCACTCTC 540
TGTGACCAAG AGTGACTCTG CTCAGCCAAC CAGGGCCTCC CTGCCCTGCG GGGCTAGGCT 600
TTCGCCATGC CACGAGCAGA TGCCGGCGTG TGGCCTCTGC AAGCTCAGAT GCCACCAGGC 660
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