| Tag | Content |
|---|
EnhancerAtlas ID | HS101-16812 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr16:30502980-30503900 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr16:30503393-30503404 | AGTGACTCATC | + | 6.02 | | JUND | MA0491.1 | chr16:30503393-30503404 | AGTGACTCATC | + | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I030491 | chr16 | 30502930 | 30503688 |
|
Enhancer Sequence | TCACTTTGTC ACCTAGGCTG GAGTGCAGTG GCACCATCTT GGCTCACTGC TGCCTTGACC 60
TCCTGGCTTT GAGCAATCCC CCTTCCTCAG CCTCCCAAAG TGCTGAGGTT ATAGCCGTGA 120
GCCACAATGT CCAGCCTCTT CCCTTTTTGT AGATGAGAAA ACTGAGGCAC AGAGGCATGA 180
AGCAATTTAC TTAACTACTA CACAGCTAGG AAGCAGTAGC ACTAGGATTT AAACCTTGTC 240
TCATGGAGTT CAAGAATTTG GAGTTCTTAA CCCTTGTGCT TCCAGACTCC ATACGACAAT 300
AGGGAAGCGG TTCCGTCTCT TCACTCTTCC TTCCATGTGC TGTAGGGCCT TGGACAGCTC 360
TGTTTTCTTC ACTCACTTTC AACTGCTCTG CACAGAGACC ATCAGATGGG GTCAGTGACT 420
CATCTCAGAG GATTCTTGCT GGTGGCTCTT GGCTCTAGCC CAATCTTGGG TCCAATTTCC 480
TGCAGTGTTT CCTCGAACAT TCAATAGAGG TTGTCCTGGT ATCTTAGAGG AAAGAACCTC 540
ATTACAGGAA GTTGAAGATG AAGACAGCCT GACACTGACA TGATATCTTT TTTTTCTTTT 600
TTTTTTTTTT TGAGACTGAG TCTCTCTGTC GCCCAGGCTG GAGTGAAGTG GCGCGATCTT 660
AGCTCACTGC AACCTCCACC TCCCAGGTTC AACTGATTCT CTTGCCTCAG CCTCCTGAGT 720
AGCCGGGACT ACAGGTGCCC GCCACCACGC CCAGCTAATT TTTTGTATTT TTAGTAGTGA 780
TGGGGTTTCA CCATGTTGAC CAGGCTGGTC TCAAACTCCT GACCTCAGGT GATCCACCCG 840
CCTTGGGCTC CCAGAGTGCT GGGATTACAG GCGTGTGCCA CCGCTCCCGG CCAACATGGT 900
ATCTTTTTTT TTTTTGAGAC 920
|
