| Tag | Content |
|---|
EnhancerAtlas ID | HS113-38673 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr9:133301470-133302690 |
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 | TGTCCCCACT CCCATCCATC CACCCCCCAC TCCTCACAGG GACACAGCTC TCTAAGCCAC 60
CCTTGTTCCA ACCTCTGGAT CCTTTCCCCA GGCCCCAGGG TGAAGGTCCA ACCACCCCAG 120
GCTGATGTTC AGGAACTGAG TCACCCCGCC CTCTTCTCCC GAGGGCACCT GCACTGAGGC 180
CACACCCAAG GAGCCAGGAA CCACTGTTGG AACCCTAGAG ACCCCCAGGA ACATGCTTTC 240
TGTTCACCCA GTGAATGCTA AAGATACATA CGTTCACATT ATTTGAGGTC CCAAAGTGTT 300
TTGAACATTG AATGAGAGAC AGTGCTAAGA GCACCGCTTT GAGGTCAGGC AGACCCCAGT 360
TCAAATCCGA GGTACACCAC TTTCTGGCTG TGGGACCTTG GGGGCAATGT CCTGGTCCTC 420
TCGGAGCTTC AGTGTTCCCA TCTGCACCGC GGGCATGACA TCGCCTGCCT TGCAGGGTGT 480
CGCCGTACAG ATGTTGTCTC TAAAACCCTA GCCTGGCACC TAGTGGCTGC CTCATCAAGG 540
CTGGCTGTCC CTACAATTTA TGTGGACCAA GCTTGTCCAA CCCATGGCCC ACAGGCCGCA 600
TGCCACCCAG AACAGCTTTG AATGCGGCCC AACACAAATT TATAAACTTT CTTAAAACAT 660
TATGATATTT TTTGTGATTT TTTTTTTTTT TTTAGCTCAT CAGCTATCCT TAGTGTTGGT 720
GTATTTTATG TGTGACCCAA GGCAATTCTT CTTCTTCCAG CGTGGCCCAC AGAAGCCGAA 780
AGATAGGACA CCCCTGATTT AGACTGCCTT GTGTCCTTCC TGCCTCCAGA ACCCAGCTCA 840
CCCCTCCCCT GCCTTTGCTT TTGCTGCCCG TCTGACGCTA TCCTCTGCCC CTCCGCACGG 900
TCTCTGTGCA TTGCTGCTAT GGTCTCAGGA GAGCCGTTTT GCACGTGTTG ACCTCCTGCG 960
TTTTATTTTA ATGGTTTTCC TGGGGCTGCC TGACTCACTG GCCAGCCCCA CTGGGAGCCC 1020
TTCAGGACAC ATTTCCTTGA CTGGGCGTGC CCTGCAGTCA TCGCCTCCAA CAGGCCTGGG 1080
CAGGAAATGG GCTTGCTGAC TCTCTGGCAC CGTCTTGGCT CTGCCTGGCT AAGCTGGCAG 1140
TGGGGGAGCT GTGAGCCTGG GCTATGGCCA GGGCAGCCTT GGGAGAGGAC ACCCTCATGT 1200
CCTTAGAGTC TATCCTCTTT 1220
|
