| Tag | Content |
|---|
EnhancerAtlas ID | HS032-00388 |
Organism | Homo sapiens |
Tissue/cell | DLD1 |
Coordinate | chr16:1346710-1347930 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr16:1347107-1347118 | GGGTGACTCAG | + | 6.02 | | JUNB | MA0490.1 | chr16:1347107-1347118 | GGGTGACTCAG | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_57892 | chr16:1347201-1347796 | VACO_503 | | SE_65650 | chr16:1346426-1347147 | Pancreatic_islets |
|
| | 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 |
| GH16I001296 | chr16 | 1346521 | 1351848 |
|
Enhancer Sequence | GACGGGGTTT CACCATGTTG GTGAGGCTGG TCTCGAACTC CTGACCTCGT GATCCACCCG 60
CCTCAGCCTC CCAAAGTGCT AGGATTACAG GTGTGAGCCA CCATGCCCAG CCCCAAGACA 120
ATTTACTTCT ATAGAAGGGT GCATCTCACG GATGGAGCAA TGGCGAGAGC ACACCTGGAC 180
AGGGGAGGGG AAGGGGTTCT TATCCCTGAC GCCGGCAGCC CCTCCTGCTG TGTGGTTCCC 240
CTATTGGCTA GGGTTGGACC ACACAGTCTA AGCTAATTCC AATTGGCTAT TTTAAAGAGA 300
GCAGGGGTAC GAGTCGGAGT GGCAGAGTGA GTAGTTTGGC AGGAAGGACA GTTATAGAAC 360
AGGTGACTCA GGATGTGTCA GGGCAGAGCA GGTGACAGGG TGACTCAGGG CAGAGCAGAT 420
GACCAGGGAA GAGATGTGAG CTACTGATTA GAACTGGTGG GAAAGTTGTT TACTGAAAGT 480
AGAGGCAAGG GAGCAAAGAA CCAGGAAGTT AAGCTTTAAA ATGGAGAATC AAAGAATAAG 540
AGAGCTGAAC AAACTGACAT GCTGATTCTT TGAAGAGAAA CTCGGAGTTC ACTATATTTA 600
ACACAGTGAG CTGATACAGT GCCACTGCAT TCCAGCTGGC AACAGAGCAA GACTCTCTCT 660
CCAGAAAAAA AAAAAAAACA GCTGTAGCCC AGACACCTTC ACACATTCTC AGGACCTCCT 720
AAGGCTGTGT CATGGCCAAA TCCTTAACCC TGGCAAAATA AACTTCTAAA TTGATTGAGA 780
CGTATCTCAA ATACTTTTTG GCTTACATAT CCTTTGTAAT AAATCTGTAA TAGTAAATAA 840
AGCATTTCCC TGAGTCCTGT GAGCCACTCT AGCAAATTGT TGGGCTCAAG AGGTGGGTCC 900
TGGGAATGGC CTATTTGTAG CCAGGTCAGA CAGAAATCGT GGGTAACCTG TGGGTAACCA 960
CAGTCCAATG CCTGGCAGGT CAGCGTACCA ATGCCAAGGG CTGTGGCAGG GAAGCGTTTT 1020
ATTTTTATTA TTTTTTTTAA GACAGAGTCT TGCTCTGTTG CCCAGGCTGG AGTACAGTGG 1080
CATGACCTCG GCTGACTGCA ACCTCCACCT CCTGGGTTCA AGTGAGTCTG CTACCTCAGC 1140
CTCCTGAGTA GTTGGGATTA CAGGTGCCCG CCACCACGCC CAGCTAATTT TTTTATTTTT 1200
ACTAGAGATG GGGTTTCACC 1220
|
