| Tag | Content |
|---|
EnhancerAtlas ID | HS133-04880 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr10:103598800-103599500 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr10:103599244-103599255 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr10:103599244-103599254 | GCCCCGCCCC | + | 6.02 | | SP1 | MA0079.4 | chr10:103599241-103599256 | GAAGCCCCGCCCCCT | + | 6.79 | | SP2 | MA0516.2 | chr10:103599240-103599257 | AGAAGCCCCGCCCCCTC | + | 7.54 | | SP4 | MA0685.1 | chr10:103599241-103599258 | GAAGCCCCGCCCCCTCC | + | 7.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr10 | 103599000 | 103599187 | | chr10 | 103599264 | 103599400 |
|
Enhancer Sequence | AGAGGCTCAG GAACCCTCAA CCCAGTCCTA AAGTACAGAA CTCCAGGTAC ACACAGTCTC 60
AGTGTCACAG AATCCCAGTG ATCACAACCC CAGGGAGACA CAGACTCAGC CATACATAGC 120
CCAGTGATGC ACAACTTAGT AATGCACAAT CCCATTAATA CACACTCCCA GAGAGAGAGA 180
AAACAGAGAC ATACAATCCT TAAGCCACAC AAGTCTATCA GTCCCATGTC ATGTATGAAC 240
TTGCTAGCTG AGTTCATGTT GGTCTAGGCC CATCTCAGGG TTTTTTCCTT CTGGACACTG 300
AACCCTTCAT CTTAAGACCC CTTCAGCCAA GAAATGCAGG AAAGGACTGA ACTTTTTCCC 360
TGCTCTGCTG CAGGCCTCCT CCTTTCATCC CTGGGAGGCG CCCTGCCCCT CAGTTAAGGC 420
CCCCTCCTCT GCCTTCGGTG AGAAGCCCCG CCCCCTCCAC CATTGTGAGG GACCTTGATG 480
CCCCTCTCCT TTCCTCTTTG AAGAGCGCTG TCTTCCTCCT GCTCAGTAAG GAGGCCCATC 540
CCCTGCTCCG CTTCTGTCCA GGATCTCGTC TTGGAAGCCC TTTCCTTGGA GGGATGTTGC 600
TCCCTCCATC TATTTGAGGG GCCCTTCCCT CCCTACCTCT GCGGAGCTCC TAACCCACTT 660
CGCTCACTTT TTGAAGGATC CTGCCCCTCC CTTCCCTTCC 700
|
