| Tag | Content |
|---|
EnhancerAtlas ID | HS121-34297 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr7:100876200-100877550 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr7:100877123-100877138 | TGAACTCCTGACCTC | - | 6.22 | | SP2 | MA0516.2 | chr7:100876540-100876557 | CCAAATCCCGCCCACCC | + | 6.29 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_28156 | chr7:100874742-100876791 | Fetal_Intestine | | SE_28156 | chr7:100876976-100884675 | Fetal_Intestine | | SE_52423 | chr7:100874627-100885461 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GACCGGAGGA CGACCCCAGT CCAGTCCAGG GGGAGGGATA GTGGGGGAGG GGGCTTAGGG 60
GAGAGGCAGG CAGGGGCTGC CCAGAGTAGG ACGGGGGCAC CAAGTCCCAG AGCAGCAATT 120
TCACTCAATT CCTTTCTCCC CACCCCAGTT TATAAGCCTT CCTCCTTCCT GGGGTCAACT 180
TCTCAGGGTA GCCCTTAGGC CCCAAGTCCA GCCCACCCAG CTCATCTCAC ACTACCTCAA 240
CCTCCTCCTG CCTCTTCTCT CTTTGGTCCC AGATCTACCT AGTTCATGCC CACCTCTAGG 300
GCCTTCATCC CATCATCTCC TCACCCAGAT GGAGCCCCAT CCAAATCCCG CCCACCCTTG 360
AAACCTTGAA AACCCAGCTG GGCCATGGGA GTCCAGGGTC GTCCTTTCCT GAAGCCAGGC 420
AGACCCCCGG GCTAGCACCA CCCTACTCAC TGGGGGCTTG TCCTCTTGCA AGCCACCTGA 480
CCTTTCTGGG CCTGTTTTAC CTCTGGAAAA CAAGCAATAC CCACCCTACC TCAAAGGCTT 540
ATTGTGAGGC AATGGGTACA GAAATGTTCT GCAAATTGAA AAGCAATGGC CAGATGGCAT 600
TGTTTTTGTT TTTTGCTGAG ACGGGTTCTC ACTATGCTGC CCAGGCTAGT CTGGAACTCC 660
TGGGCTCAAG GCAGTTCTCC TGCCTTGGCC ATTTTTTTTT TGACAGTCTC ACTCTTTCAC 720
CCAGGCTGGA ATGCAGTGGC ACAATCTTGG CTTACTACAA CTTCTGCCTC CCAGGTTCAG 780
GTGATTCTCC TGCCTCAGCC TCCAAGTCAG TGGGACTACA GGTGCCTGCC ACCACGCCTG 840
GCTAATTTTT TTTTTTTTTT TTTTTTTTTT TTTTTGGTAT TTTTAGTAGA GACAGGGTTT 900
CACCATGTTG GCCAGGCTGG TTTTGAACTC CTGACCTCAA GTAATCCACC CACCTCAGCC 960
TACCAAAGTG CTGGGATTAC AGGCATGAGC CACCATGCCC CGTGGTATGG CACTGTGGAC 1020
GTGCACTGTG TGTGTGCGCC ATAGCGTGCA CCCTAACTCT GCTCCCCAGC TAGGATGTAA 1080
GCTCCCGGAG GCAGCCGCTC ACTCTTATCT TCGAAGTCCC TCCCACACCT GGCCGTGGCC 1140
AGCCCCTACT GGGAGCTCAA GAAACACTGC CGATGGGCTG ATTTGCAGCC AGGAGATCTG 1200
GGGAGTACAG ATGAGGCAGG GGTGAGCAGG TGTCCATGCA GCAGGGTAGG GGAGGTGAGC 1260
ATGAGGAGTG GGAATTGGAG AGGAGATTAG ATGAGGACAA AGCAGCCTGA AGTCTGCGGT 1320
TGAGGGGGAC CCCCGCCCCA TCACCTTCCC 1350
|
