| Tag | Content |
|---|
EnhancerAtlas ID | HS101-17664 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr16:89322480-89324120 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr16:89322501-89322516 | GAGGTCAGGAGTTCA | + | 6.22 | | RREB1 | MA0073.1 | chr16:89323632-89323652 | GGGGGTGTGGTGGGGGGTGG | - | 6.22 | | RREB1 | MA0073.1 | chr16:89323757-89323777 | CGTCTGGGGGTGGTTTGTGC | - | 6.26 | | Zfx | MA0146.2 | chr16:89323547-89323561 | CAGGCCTCGCCCGC | - | 6.65 |
|
| | 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 |
| GH16I089256 | chr16 | 89322877 | 89324252 |
|
Enhancer Sequence | GCTGAGGCGG GCGGATCACC TGAGGTCAGG AGTTCAAGAC CATCCTGGCA ACGTGGTGAA 60
ACCGTGTCTC TACTAAAAAT ACAAAAATGA GCCAGGCATG GTGGTGGGCG CCTGTAATCC 120
CAGACACTCG GGAGGCTGAG GCTGGAGAGT CACGTGAACC CGGGAGGTGG AGCTTGTAGT 180
GAGCCGAGAT TGCACCACTG CACTCCAGCC TGGGCGACAG AGCAAGACTC CATCTCAAAA 240
AACAAACTAA CTAGGGCCGG GCGCCATGGC TCTCGCCTGT AATCCCAGCA CTTTGGGAGG 300
CTGAGGCAGG CGGATCACAA GGTCAGGAGA TCGAGACCAT CCTGGCTAAC ATGGTGAAAC 360
CCCGTCTCTA CTAAAAATAC AAAAATGAGC CAGGCGTGGT GGTGGGCACC TGTAGTCCCA 420
GACACTCGGG AGGCTGAGGC AGGAGCATGG TGTGAACCCG GGAGACGGGG CTTGCAGTGA 480
GCCGAGATGG CGCCACTCCA GCCCGGGCGA CAGAGCGAGA CTCCGTCTCA AAACAAAACA 540
AAACGAACTA ATTAAACAAA ACAACAAAAG AAAACCTGGC ATCAGTCCTG GTCACTGTGC 600
TCACGCCAGC CTCTCCATCC CGGCTCCTCT TCCAACTCTG CTTCCTGCTT CAGTGACTCG 660
GATGTCGCCC TTCGCCCCAT GCCCAGGAAA CCGGAGGTGG CAGTGGGGGA AGGGAGGGAG 720
GCGTGGAGAA GATACCCTGT CACCATCTCC ATGCCCCTCC CCGGGACCAC ACAGGTCGCC 780
TGGGCCCTGA CCAAATGGTT CGTTGTCCGC CAAGCCAGAC AGCAGGGCAG GCGCGCTCTG 840
TGCAAAACCG AGTCGTGTGC GGGCCCAGGG TGGCGCTCGG GGCGCTTCCA GCGCACGTCA 900
CCTCATCTGC GTCGTCACCA CTGTCGCCTC CGAAAGCGCA TTCCGTCGTC AAAATACACC 960
ACGAGGTCCC GGGTGCCCTC ACCGCCCTCC CCTTCCTCGC CCTCTCGTCG TTGCTGTTGG 1020
GACGGGCTCT CGTCGCCCGC GCTGGGGCGC AGTGACTCAG TGTGACTCAG GCCTCGCCCG 1080
CGCTCGGGCT CACGGAGCAG CTGGGACGAC GGGCGTGAGC GCAGAAGCCG CAGAGCCCCT 1140
CGCGCGCCTC GCGGGGGTGT GGTGGGGGGT GGCCGCCTCC GGGGACGGGC GGGCTGCGGG 1200
GCTCCGACCC CGCGGCAGCG TCTCGCGGCG CCTGAGGCCC CGGTGGGCGT GGGTTCCAGG 1260
CTGCACGGCT GGTTTGCCGT CTGGGGGTGG TTTGTGCTGG GACCCCCGCC TCGCCGCAAG 1320
GACCGACGCT TTCCGTATCC CGGGTTCCTG CTTCGGTGTA CCGGCAGAAT CTGATCACGC 1380
GTGGCCTGGA GAATGCGCCC AGGGTCGTAT TGCCTGGAAG GAGCTCTCAG CCGCTGGGGG 1440
AGCCGGAAGG GAGACGGTTC TGCCCTGGAC GCGGGCTGCT CGGCGGCCCC GGCTCTCCTC 1500
CAACCGGCCA AACCCCGCCT GGTCCCGCCG CCGGTGGCTG CTGCTCCCTC GCCGTCTTCC 1560
TGCCGAGCAG CCGCTGGCGT CTTCTTCCAC TGATCTGCTC CTCTCCACGT CCGGCTGCCT 1620
TGTCGGCCTG CTAGGGTCTT 1640
|
