Tag | Content |
---|
EnhancerAtlas ID | HS023-12119 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr19:2517700-2519000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr19:2518303-2518314 | GATGAGTCACC | - | 6.32 | JUND | MA0491.1 | chr19:2518303-2518314 | GATGAGTCACC | - | 6.62 | SREBF1 | MA0595.1 | chr19:2518719-2518729 | GTGGGGTGAT | - | 6.02 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_37152 | chr19:2517403-2519110 | HSMMtube |
|
| 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 |
GH19I002518 | chr19 | 2518281 | 2518430 |
|
Enhancer Sequence | GGTCTCACTA TGTTGCTCAG GCTGGTCTCG AACTCCTAGG CTCAGGCGAC CCTCCCGCCT 60 AGACCTCTGA AAGTGCTGGG GTTACAGGCA TGAGCCGCCT CGCCTGGCCA GTACCTCTGC 120 ATCCCAGATC CTCTGTCCTC CTTTGGACCC CAAGGATACC TGGGACCTGG GCCCTTCAAA 180 CGGCCAGGAG CCTGTGGGAC AGCTTTGGGG TCTTGCCCAG CTGGGCAGCC GGGGGACGCT 240 CATGCCCACA GAGTGAGCCC GCCGGCTGCG GCCTGTGATG ACTCGGACCT GGCCTGCTTT 300 CTAGACTTCT ATTTGGGAAG CGGCCCTCCT GGACGACAGA AATAGCCTCC AGACCCCGAA 360 AATAGCTGGC ATTGTGGCTC CAGCACGTGG CACCTTGGCA CCACCCCCCA TGCCCACTGC 420 GCTGGGCTGG TGAGCCCCAA GATCGTCGCC GTTGAGGTTC TGTGGTTCTG GTCGCCGCGT 480 TGGAGCTGGG GATGTAAAAC CTCAGGCGGG ACTGGGAGTG GGGACGGGTC AAATCCTGGC 540 TCCCCCCGAG GCCCGACATT CAAAGGGGCG GTGGGGGCCC CTCCTCAACA TCAAACAGGG 600 CAGGATGAGT CACCGCCCTC CGCCCGGGCT GGGGGCTGGC ACCCACTCGT AAAAGGAAAA 660 CCACTTCAAC CAGGGCTTTC TCTCTTTTCA GCCCGAAGGA ATGCTTTGAA TGCTCAGGTC 720 TGTCCTCAGC AGTCAGATTG CTGGAACATT CAGACACCTC GTGGGAGGCA GACCCCTCCC 780 CTACTGGTTG GATCCCGGCC AGCAGCAGCG TGATGGGGTC TGGGAGGGCT CAGAGCTGCG 840 CTGGAGGGAG ACTCACCGGC CGATCAGAAC CACCTGTGCC ACCTGGCCAG CAGGGACGAC 900 TCTGTCCGCC TCCCCGCTGG GAGCAAAGCA AGGGCCGGTC ACCCCTTCCT AATAAATTCC 960 CGTGGCCAAT AATGACAAGC TGGTGACAGG TGCTGGAGAG CTGAGTTCTG AGTGGATACG 1020 TGGGGTGATG GCTGATTTTA TGGGTGCACT AGGGCGGGCC ATGGTGCCCC AGGGTTTGGT 1080 TAAATGTTTT TTTGTTTTTG TTTTTTTTCT GAGATGGAGT CTCACCCTGT CGCTTGGGGT 1140 TGGAGGGCAG TGGCGCAATC TCAGCTCACT GCAACCTCTG CCTCTCGGGT TCAAGCTATT 1200 CTCCTGACTC AGTCTCCCAA GTAGCTGGGA CTATAGGAGC CTGCCACCAC GCCTGGCTAA 1260 TTTTTTTGTA ATTTTAGTAG AGATGGGGTT TCACCATATT 1300
|