| Tag | Content |
|---|
EnhancerAtlas ID | HS184-15377 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr19:19701750-19702560 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr19:19702034-19702048 | GAGAGGTGACTCAT | + | 6.35 | | LMX1B | MA0703.2 | chr19:19701796-19701807 | GTTTTAATTAA | + | 6.14 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_12109 | chr19:19700241-19703035 | CD3 | | SE_18839 | chr19:19700276-19704898 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19648 | chr19:19700122-19703992 | CD4p_CD25-_Il17p_PMAstim_Th17 |
|
| | 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 |
| GH19I019589 | chr19 | 19700502 | 19703700 |
|
Enhancer Sequence | AAATGTGGCT GGTGTGGCTG AGGAATGCAC TGGTTAATTG CATTTGGTTT TAATTAATTC 60
AAATGTAAAC AGCCCTGCGT TGAGTATCTG GAGCCACCCA GCTGATGAGA CTCAGGGGCT 120
CAATTTGTGA GTTACCCTGA GACTGAGGGG AGGAAAGGAT ACTCCAATCA ACCTGGAGAA 180
TAAGTCCCCC AGCTGCCGGG GTCTACTCCC ACAAGAACCC TAAAGAAATG TACATGGGAC 240
TCAGCCCCAG GGTACAGCTA ATTAGAAAAA GGATCTCAGT TCCAGAGAGG TGACTCATAG 300
GCCTCAGGGT GACTGCTAGG ACCCAGGAAA GCCCCATGAG CACCATGACA CCCCAGCTTC 360
CTGGCTGAAT TTACAGAACC CGATTCTGTA ATTGCAACAG ATCCGACCAG CTGACGAGGA 420
AGGGAAAGAA TGAGAATGGC TTATGCCTGC CAACTACTAG CAAGGCCAAT CATTAGTCAG 480
GAAGACAAAA AGGCATTCCC TGATGTTATG CATTATTTAC ATTTACTCCT CTGAATGGGG 540
CTCTGTGCGT TCCTACAGCA CAGCAAGGGT TCCTGCAGCA CAACAGCCCT GGCTGAGAAA 600
CTTCTTGTTC CCCAGAGACA CAGTCACAGG GTGGAGAAGG CAAAGCAGGC CCCTTCTCAA 660
GAACGGCCCA GGATGGGATG GCCGAGTGGG TCTGCAAGGG GCCTCTGGGG CTCAGCACAC 720
CGCCTCGGAG CTGCCTACCC ACTCGAGATC TGAGATCCGA AGCTTTTCAC ACAAGCTGTC 780
ACTCATGCTC ATGTGGAGGT AAAGCCTGAC 810
|
