| Tag | Content |
|---|
EnhancerAtlas ID | HS121-19887 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr19:18556070-18557110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr19:18556310-18556324 | GTGGGGGCGTGGCA | - | 6.19 | | KLF16 | MA0741.1 | chr19:18556312-18556323 | GGGGGCGTGGC | - | 6.62 | | RREB1 | MA0073.1 | chr19:18556355-18556375 | GGGGAGGGGGTGGGGGGGTG | - | 6.49 | | RREB1 | MA0073.1 | chr19:18556344-18556364 | CGTGGGGGGGTGGGGAGGGG | - | 6.4 | | SP3 | MA0746.2 | chr19:18556311-18556324 | TGGGGGCGTGGCA | - | 6.41 | | SP8 | MA0747.1 | chr19:18556311-18556323 | TGGGGGCGTGGC | - | 6.11 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_24446 | chr19:18556373-18557100 | Colon_Crypt_2 | | SE_29898 | chr19:18552817-18556250 | Fetal_Muscle | | SE_41560 | chr19:18556361-18558683 | LNCaP |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH19I018442 | chr19 | 18553762 | 18556350 | | GH19I018445 | chr19 | 18556467 | 18558694 |
|
Enhancer Sequence | CGAGTAGTCT AGAAGAAAAA CAAAATTTTG AGAAAACAGA ATGTGTCCCC GCCTACAGGA 60
AACCCAAATT GAGTGGTCCC AGGTGCTCTG AGAAGGGGGC ATGGGAGGGT GGGGCAGCCT 120
CAAGGACAAG GCCAAGTAAC ACCCCAGGGG CCCACAGCGG CTGTAGCTCC GGAGTGGGTG 180
GGGCATGAGG GAAAGGCTGC CGGGTCCCCT GGAGGCAATA GCAGGTGGGG CACTGCTGTT 240
GTGGGGGCGT GGCAGGACAA GGAAGTATCC ATGTCGTGGG GGGGTGGGGA GGGGGTGGGG 300
GGGTGCAGCA AAGAGGGAGG GAAGGGGAAG GAGAGATGCC CCAAGAACCC GTGGCTCGCA 360
GCCCCTAGAA CCCCATCATG AGTCGTCGTC TTTGGAAGGC AAAGGGGCCT TGGCCAGGAG 420
AGACCCCGGC ATCTGATTAA TCAGGGCCCA GCCCTGTAGT CAGGTCACCA GTTCCGAAAG 480
GTGGCAGGTG GGGCGGCTAC GTCCAAGGCT AGGCTAAGGG TGGAGACTCT CTGTATACAC 540
AGGGCAGCTG AATGAGCTGT GAGCTCAAGC CAGGGGACCA CAGGAGTCCT GATTCCCAGG 600
ACCACAGGGA CCTGTCACCT CCCCCTGCTA TAGTTGTGGC AGCATGGATG GGCCCCAGGG 660
TGCTGGACAG AGCTCAGCTG CGGAGTCTCC TGAGGGTTTG GCACAGGTAC CAAGAGCCCT 720
GTGTCCTAGG CTGTGAGAGG ACCCCAGGCG CTCAAACATG TGGGGATCCA TGTACCCCGG 780
CTCGCCCCCA TCCAAGGAGG TGGGTCACAG CTGTCCCCAC TGCAAAGGAG GCTGACAAGC 840
TGGGCTGCCT TCAAGGACTC CCACAACAGG ACCCCAGGGC CGGGCCAGAA CCATGGGGTT 900
GCTGCATGGA GTGCACCAGG GGGAGAAGCG CTGCCTGGGG AAGGGCCAGA CTCTGGGGCC 960
ACCAAGCTCG TGGTGGCGAT GGTGCGCGCC CAAGTGGGCC CTGGCTCCCG CCAGAGCCAG 1020
GGCACAGTAG GCAGCGGGGG 1040
|
