| Tag | Content |
|---|
EnhancerAtlas ID | HS002-10129 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chrX:49040520-49041070 |
Target genes | | Number: 18 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chrX:49040861-49040872 | GGGGGCGGGGC | - | 6.02 | | KLF16 | MA0741.1 | chrX:49040921-49040932 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chrX:49040862-49040872 | GGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chrX:49040922-49040932 | GGGGCGGGGC | - | 6.02 | | Klf1 | MA0493.1 | chrX:49040542-49040553 | AGGGTGTGGCT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCAGGAGGTG GGCCTATGAG CCAGGGTGTG GCTGGGCTGT GAGCCAGAGG ACAGGTCGTG 60
GGGAGTGGGA TGCTTTGTGG GGGAACTTTC ACTAGACACA GGCATCTAAC CTGTGGTGAG 120
GCTCTGAACT TGTGGGCTCT GAGCCTGTGG GTAGGGCCTG AGTCTGGGGG CTGTAGGCTC 180
TGTTTATTGG GTGCAGGGCT CCAGCAGGAG GATAGGACGC TGGGCCTGGG AGAGTAGGTC 240
TGAGTCTAAG AGGGGTGCTG GAGGCCAGAG GGCGGCGCTC AAAGTTAGAG ACGAAGAATC 300
TCCCTAGGGA TGCGACTCCG CGGCTACGGG AGAACACTTC TGGGGGCGGG GCTGCGTAGT 360
GGGTGGAGCT CTCCTGGGAA AGGACTTTGG GGAATGAGTC AGGGGGCGGG GCTCTGAATC 420
TGAGCCTGAG GCTCTTTTCC CAACTGAGAT CCCTCTGTAG GCGGAGCTCA AGCGTAGGGG 480
CGTGGCGTAA GGCTCCTGGA TTTCCCCCCG AAGGCGGAGC TCTGACAAAG GCGAGGCCCT 540
TTAGGGGCGC 550
|
