| Tag | Content |
|---|
EnhancerAtlas ID | HS048-30209 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr5:138774240-138775090 |
Target genes | | Number: 17 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr5:138774862-138774873 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr5:138774863-138774873 | GGGGCGGGGC | - | 6.02 | | Myog | MA0500.1 | chr5:138774831-138774842 | GACAGCTGCGG | + | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGGGCAGAGC ACTCATGTCT TCTCTGGAGG ACCTGAGAAA GGCTTTAACA ACATCTTTCT 60
TCCGCTTAAC ATCCCTCAGC TACCTCCACC CACTGCTCCT GGACAGTCTT CCTCTAAGTC 120
GGCCTGGCTA ACTCCGACGC ATCCTTCTTG TCACCATTTG TAACACTTTC TGCAAGAAAC 180
CTCCCTTGAC AGCCAGTCTG CGTTAGGTAC CTTGTAAGTG TGCTCTCCAA ATCCCTGACC 240
TTGCTGTGTA GCCCAGGCGT TTTGTATTAT TCGCCCGTTT TGTAATTGGC TGTTCAGTCG 300
TCAAACTCTC TCAGTGGGCT GCGAGTTTTG TGAGCTAAGG GACCCATGTC AGTCAAATCC 360
CCACTGCAGA ATCAGCATTA GGCGGGGCAC ACAATAGGTA TTGGATCAAT ATTTTTTGCC 420
TGACTGTAGG GTGGAAAAGG CTGGTCCTGA TGCCGGCTGG AGCGACATGA TCAAACAGGG 480
ACTGAAGGTC AGGTGGCCCA GTTAGGCGAA AGATAAGGGC CAGGTTAGCA AGCTGCGGAG 540
AGACCGCAGC ACCCCACGGG CCCTCCAGTC ACCTTGGCAT GGGCGGGGCC TGACAGCTGC 600
GGGCCCTGGG CGGGGCACGG GCGGGGGCGG GGCTGGGGGC CGGAGGCAAC AAGTCGTCAC 660
CGGTGACTCT GGGCTCGCGG TCGGTCCCCA GCTTCCCTAC CCCATCCGCA ACCCTACTCA 720
GGCTCAGCAT CTTTTCACAG GCCTCTATCC ATCACCTCAG ACCCAGGATC TCAGCCCTTG 780
TGCGTCTTCA GGATCCTCAT CCCTGATCTC TCCCGAAGGC CGCCCTATCC CTCCTTCAGG 840
CGGGGACCTA 850
|
