| Tag | Content |
|---|
EnhancerAtlas ID | HS048-38767 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chrX:49040450-49041070 |
Target genes | | Number: 25 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chrX:49040508-49040519 | GGGGGCGGGGC | - | 6.02 | | KLF16 | MA0741.1 | chrX:49040861-49040872 | GGGGGCGGGGC | - | 6.02 | | KLF16 | MA0741.1 | chrX:49040921-49040932 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chrX:49040509-49040519 | GGGGCGGGGC | - | 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: 2 | Chromosome | Start | End |
| chrX | 49040473 | 49040600 | | chrX | 49040631 | 49040941 |
|
Enhancer Sequence | GGGGACATAC AGATTATCAC CACCAAAGGT CTGTGAGCAG GGACAGGGAT CTGGGCCTGG 60
GGGCGGGGCT GCAGGAGGTG GGCCTATGAG CCAGGGTGTG GCTGGGCTGT GAGCCAGAGG 120
ACAGGTCGTG GGGAGTGGGA TGCTTTGTGG GGGAACTTTC ACTAGACACA GGCATCTAAC 180
CTGTGGTGAG GCTCTGAACT TGTGGGCTCT GAGCCTGTGG GTAGGGCCTG AGTCTGGGGG 240
CTGTAGGCTC TGTTTATTGG GTGCAGGGCT CCAGCAGGAG GATAGGACGC TGGGCCTGGG 300
AGAGTAGGTC TGAGTCTAAG AGGGGTGCTG GAGGCCAGAG GGCGGCGCTC AAAGTTAGAG 360
ACGAAGAATC TCCCTAGGGA TGCGACTCCG CGGCTACGGG AGAACACTTC TGGGGGCGGG 420
GCTGCGTAGT GGGTGGAGCT CTCCTGGGAA AGGACTTTGG GGAATGAGTC AGGGGGCGGG 480
GCTCTGAATC TGAGCCTGAG GCTCTTTTCC CAACTGAGAT CCCTCTGTAG GCGGAGCTCA 540
AGCGTAGGGG CGTGGCGTAA GGCTCCTGGA TTTCCCCCCG AAGGCGGAGC TCTGACAAAG 600
GCGAGGCCCT TTAGGGGCGC 620
|
