Tag | Content |
---|
EnhancerAtlas ID | HS183-14023 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr9:133301310-133302690 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr9:133301811-133301826 | AGGTCAGGCAGACCC | + | 6.12 | FOSL2 | MA0478.1 | chr9:133301605-133301616 | CTGAGTCACCC | - | 6.02 | JUNB | MA0490.1 | chr9:133301605-133301616 | CTGAGTCACCC | - | 6.02 | Klf1 | MA0493.1 | chr9:133301647-133301658 | GGCCACACCCA | + | 6.62 |
|
| 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 |
GH09I130424 | chr9 | 133299788 | 133303090 |
|
Enhancer Sequence | GGTGAGGCCC CTCTGCTTTG TTCCACCCCC ACTGCCCCAG CTAAAACCTG CCAGGGGGCC 60 CAAATGCACG TGGCTGGAAT CCACCCCTGC CCCTAACATC CACTGACCAT GGGCCAGAGA 120 CTTCAGACTG AGACGGCCCG GCTGGCCTAC TCACCTGGCC TGTCCCCACT CCCATCCATC 180 CACCCCCCAC TCCTCACAGG GACACAGCTC TCTAAGCCAC CCTTGTTCCA ACCTCTGGAT 240 CCTTTCCCCA GGCCCCAGGG TGAAGGTCCA ACCACCCCAG GCTGATGTTC AGGAACTGAG 300 TCACCCCGCC CTCTTCTCCC GAGGGCACCT GCACTGAGGC CACACCCAAG GAGCCAGGAA 360 CCACTGTTGG AACCCTAGAG ACCCCCAGGA ACATGCTTTC TGTTCACCCA GTGAATGCTA 420 AAGATACATA CGTTCACATT ATTTGAGGTC CCAAAGTGTT TTGAACATTG AATGAGAGAC 480 AGTGCTAAGA GCACCGCTTT GAGGTCAGGC AGACCCCAGT TCAAATCCGA GGTACACCAC 540 TTTCTGGCTG TGGGACCTTG GGGGCAATGT CCTGGTCCTC TCGGAGCTTC AGTGTTCCCA 600 TCTGCACCGC GGGCATGACA TCGCCTGCCT TGCAGGGTGT CGCCGTACAG ATGTTGTCTC 660 TAAAACCCTA GCCTGGCACC TAGTGGCTGC CTCATCAAGG CTGGCTGTCC CTACAATTTA 720 TGTGGACCAA GCTTGTCCAA CCCATGGCCC ACAGGCCGCA TGCCACCCAG AACAGCTTTG 780 AATGCGGCCC AACACAAATT TATAAACTTT CTTAAAACAT TATGATATTT TTTGTGATTT 840 TTTTTTTTTT TTTAGCTCAT CAGCTATCCT TAGTGTTGGT GTATTTTATG TGTGACCCAA 900 GGCAATTCTT CTTCTTCCAG CGTGGCCCAC AGAAGCCGAA AGATAGGACA CCCCTGATTT 960 AGACTGCCTT GTGTCCTTCC TGCCTCCAGA ACCCAGCTCA CCCCTCCCCT GCCTTTGCTT 1020 TTGCTGCCCG TCTGACGCTA TCCTCTGCCC CTCCGCACGG TCTCTGTGCA TTGCTGCTAT 1080 GGTCTCAGGA GAGCCGTTTT GCACGTGTTG ACCTCCTGCG TTTTATTTTA ATGGTTTTCC 1140 TGGGGCTGCC TGACTCACTG GCCAGCCCCA CTGGGAGCCC TTCAGGACAC ATTTCCTTGA 1200 CTGGGCGTGC CCTGCAGTCA TCGCCTCCAA CAGGCCTGGG CAGGAAATGG GCTTGCTGAC 1260 TCTCTGGCAC CGTCTTGGCT CTGCCTGGCT AAGCTGGCAG TGGGGGAGCT GTGAGCCTGG 1320 GCTATGGCCA GGGCAGCCTT GGGAGAGGAC ACCCTCATGT CCTTAGAGTC TATCCTCTTT 1380
|