| Tag | Content |
|---|
EnhancerAtlas ID | HS101-02762 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:153494880-153495730 |
Target genes | | Number: 19 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYB | MA0502.1 | chr1:153494933-153494948 | AAATGCACCAATCAG | + | 7.1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CTAGCTAATC TGGTGGGGAC GTGGAGAACC TTTGTGTCTA GCTCAGGGAT TGTAAATGCA 60
CCAATCAGCA CCCTGTCAAA ACAGACCACT CCCGTCTACC AATCAGCAGG ATGTGGGTGG 120
GGCCAGATAA GAGAATAAAA GCAGGCTGCC CTAGCCAGCA GTGGCAACCT GCTCGGGTCT 180
CCTTCCACAC CGTGGAAGCT TTGTTCTTTC GCTCTTTACA ATAAATCTTG CTGCTGCTCA 240
CTCTTTGGGT CCACACTGTC TTTATGAGCT GTAACACTCA CTGCGAAGGT CTGCAGCTTC 300
ACTCCTGAAG CCAGTGAGAC CAGGAACCCA CCAGGGAGGA GGAACAGAAC TCCAGATGCC 360
CCGCATTAAG AGCTGTAACA CTCACCACGA AGGTCTGCAG TTTCACTCCT GAGGCAACAA 420
GACCACGAAC CCCACCAAAA GGAAGAAACT CTGAGAACAC ATCCGAACAT CAGAAGGAAC 480
AAACTCCAGA CATGCCGCCT TTAAGGACTG TAACACTCAC CGCGAGGGTC TGCGGCTTCA 540
TTCTTGAAGG CAGTGAGACC AAGAACCCAC CAATTCCAGA CACAATAGCC TCCCAGGCTG 600
GGTGCAGTGG CTCACAGTCT GTAATCCCAG CACTTTGGGA GGCCAAGGCA GGTGGATCAG 660
CTGAGGTCTG GAGTTCAAGA TCAGCCTGGC CAACATGATG AAACCCCATC TCTACTAAAA 720
ATACAAAAAT TAGCCAGGCA TGGTTGTGGG AGCCTGTACT CCCAGGTACT GGGGAGGCTG 780
AGGCAGGAGA GTCACTTGAA TCCGAAAGGT GGAGGTTGCG GTGAGCTGAG ATCACACCAC 840
TGCACTCCAG 850
|
