| Tag | Content |
|---|
EnhancerAtlas ID | HS121-20519 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr19:43966000-43967270 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr19:43966320-43966330 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr19:43966320-43966330 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr19:43966320-43966330 | ATTTTCCATT | + | 6.02 | | Sox3 | MA0514.1 | chr19:43966376-43966386 | AAAACAAAGG | - | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_17644 | chr19:43966063-43969257 | CD4p_CD25-_CD45RAp_Naive | | SE_26835 | chr19:43964356-43970776 | Esophagus |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TGCAGGAAGG AGACACAGAT AGGTCAGTGG CTGGAGGGAG AGAGGTTGAC ATGGCCAGAA 60
CAAAACTTAG AGGCATCAGA CAAGAACAGA GAACCTGACC GGGCGTGGTG GCTCACGCCT 120
GTAATCCCAG CACTTTGGGA AGCCGAGGCA GGTGGATCAC TGGGCAACAG AGTGAGACTC 180
TGTCTTGCAA AAAAAAAAAA GAACAGAGAA CCCCCAAAAT GAGACAGAAA GTCTCTGCAT 240
CCATTAATCC CAAAATCTCA ACTCAGGTCC TACTATGAGA AACAGACAGA CTCACTGTCT 300
TTGGCACATG GTGGATTAAC ATTTTCCATT GTGCTTTGAA TGGAAATGTG TGTAGGCTGA 360
ACCAAAAGTA GGGTTTAAAA CAAAGGCTTA GACTGAGATA CAAGACCTCT CACAAGACCA 420
CAGTGCAGAA CAAACTTCCT CTACAACCCT CTCACCATTA TCCCCTTAGC CTTCACCCTG 480
GCTTTTACCT CCCCATCAGA ATTTACTCTT AGAGTCAGAG TTACATCTCC ACACCAGGCT 540
CAGTGGTTCA CGGCTGTAAT CCCAGCACTC TGGGAGACCT AGGCAGGGGG ATCTCTTAGC 600
CCAAGAGTTC AATACCAGCC TGGGTAACAT GGCAAGACCC CACTGTTACC AAAAATAAAA 660
GGAACCAGTC GTGGCGGTGC ACCCTGTAGT CCCAGCTACT TGGGAGGCTG AGGCGGGAGG 720
ACTGCTTGAG CCCAAGAGGT AGAGGCTGCA GTGAGCTATG ATTGCGCCAC TACACTCCAG 780
GCTAGGCGAT AGAGCAAGAT GCTGTCTTTA AAAAAAAATA GTAATAATAA AATAAAAAAG 840
AACTACATCT TCCATAGCAT AACTGGCAGG GGATGGGATT TGAAGAACTT CATTTTCCAT 900
GGTTACATTT CTCAATAGTC TGGGACAGGC GGGGGACCCC TTGAGTTTTA AGGGCTAAGA 960
ACTAGAGATT CCCCGCAGTG CCTGGGCAGA AGCTTAGAGG CTTAAATACC TCTTAAGTAC 1020
CTGGCAGCCC TCTATGGAAA TGCATTTCCC TCCAAAACAC TCTGGGACAA AGCATCACTA 1080
TCCCCACACT ATTAATATGT TGGGGGAAGG GACTGCATTT TCCATGATGC CCTACGATAC 1140
AAGCACCTAG GCCCCACGAT TCCCAGAATG CGTCGCAGGT TAAGGAAACG CTTTGGGTAA 1200
AGGGCTCCCT ACCGCCCAGG GTGCTTCAGA AGGGCTACCA CAACTCCCGT AGGTCCCGTG 1260
CTCCGGGGCT 1270
|
