| Tag | Content |
|---|
EnhancerAtlas ID | HS139-57452 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr9:133301310-133302690 |
Target genes | |
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
|
