| Tag | Content |
|---|
EnhancerAtlas ID | HS121-11503 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr14:103999190-104000880 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr14:103999875-103999886 | CCACACCCTGC | + | 6.62 | | NR2C2 | MA0504.1 | chr14:104000853-104000868 | TGCCCTCTGACCCTC | - | 6.66 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_04042 | chr14:103999622-104001771 | Brain_Anterior_Caudate | | SE_05960 | chr14:104000109-104002743 | Brain_Hippocampus_Middle | | SE_07063 | chr14:103999188-104001357 | Brain_Hippocampus_Middle_150 | | SE_24782 | chr14:103998190-103999988 | Colon_Crypt_3 | | SE_26871 | chr14:103998538-104004355 | Esophagus | | SE_54593 | chr14:103996750-104012040 | Stomach_Smooth_Muscle |
|
| | 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 |
| GH14I103532 | chr14 | 103999139 | 104004361 |
|
Enhancer Sequence | TCCGGGGTTC CGGGAGAGGT ACAGCCTGGG TGGGGGTGGG GCAAGGGTGC AGGACTGAGC 60
TCCTGGGATC TCAGAGGGGT CCAGAGACCA AGCCACACCA TGGCAGTGGC CAGGCCAGGG 120
CCCCACTTTG GCCTGAGGTG AGGAGTGGGT CAGGCTGGCC AGGGGAGGCA GAGCTGGGGA 180
GGATGGTCCC TGGCTGGGCC CTGCTCCTGG TCTCTGGCCT CTCCCAACCC CCTGATGGAG 240
GAAGGTGGCA GCGCCACCCA AGTGCAGGGC AGGCCCGGCC GGAGGAGTCT GGAGTCCCCT 300
CCCTGCTGTT TCCCAAAACC TCTCCTCCCC CAGGCTCTGG AGCCCAGGGA GCTGGCCCCT 360
TTTAGGGAAG ATGCTGGGTG CGGAGGCGGG GCAGCCCTGG GGAAGGTCGG GCCTCAAGCC 420
AGGGAGGTGG CTGGGAGGCC CAGGGTTTTT CCCTTTTCTG GAGAAGGAGC AGCTCAGGCA 480
GCAGGGGCCC CTTCCTTCTT CCCAGCTGAG AGTTGTATTC TGAGAGGGTT GAAGGGTGGA 540
GGTGCTGGGC GCCCCACCCC ACCTCAAAGA TGAGCCGAGG CCTGGTGCGA ACAGCAAGGC 600
TGTGGCCGGG GGTCCCCTGC TGGCTCCAGC CCAGCCCTGA CTCCTGGGTC CTGGTCTCTG 660
CTGAGGTGGG TAGCTGTGGG GATCTCCACA CCCTGCCTCC TAGGCTTCCT GCTCTGGGGA 720
CACTTCTGGG CCTGGACCAT AGTCCCAGGG AGGCTGAACC CGGCAGAGCC TCCCCTGGGG 780
CCCCCCTGCT GCCTTTGTGA CTCCTTCCTC CAGCGTGGCT CGGGGAACCC GCGCCTGCCT 840
CTGGGACCTG TCCCTTTCCC TGCGAGCTCC CCCTTCTGGG TCCAAAGGCT CCTGGCTCAT 900
TCATGGGCCC GGCATCTCCT GCCGGCCACG GGAGCCCGCT GGGGAGGATG CGGCATGCTC 960
AGCCTCTGTG CCCTGTCTAG GCTGTTGTCA CACAGCAGGT GCCTCCTCTA ACCCCGAACC 1020
TCCTGGCGGC CCCGTGTTAG GGTACAGCTG AGGAGACCAA ACCTCAGGGA CGTTTGAGGA 1080
CACTTGCCTG GGCCACATAC CTCTACCCGG CCCTGGCTTC CCCAGGTCCT CCCTGCCAGG 1140
ACAGGGACCC GGGCTGGGTT CTCATTCACT GCAGGCCAGG CCAAGTGAAG CCCGTGGCTG 1200
CCCTGGTGGG AGGCGGCAGG GAGGGGCTGT CATGCTCGGG CTCTGCTTCG AGTAGGCGCC 1260
TCCTGTTCCC GGGAGCAGCG ACAGCCTCTA ATTTCCTGTG ACAGCAGCGG CCCCCGCACC 1320
GCCCCACGCT GCCGTGCTGT CAGAGCTGCT CCGGGCCCAG AGCTCCAGCA GCCCTGTGGA 1380
AGGCAGGAGA GCAGTGCCCG CTGTGGGCCA AGTGAGACAA TGGCAGCGCG GGCTTGACCC 1440
GGTGCCTGGC ACATGGGAGG GCCTGGCATG GCTAAGCTGG GTGACATGAA CAGCGGCGCC 1500
AGGCCCCATG GGGGGCTGTC AGTTGAGGGC CAGGCCCCTC TGCCCTGCAG TCCCAGCTCT 1560
TGGAGAGCTT GCAGTCTGTG TTGGGGCTGT CTTAGGCTGG CCTCAGACCC TAGGGTGGGA 1620
GTCCAGGGAT GCTAGGGCCA GACGGGCCAG GCTCTGCCAC CCCTGCCCTC TGACCCTCGG 1680
GTCCTGTTTC 1690
|
