| Tag | Content |
|---|
EnhancerAtlas ID | HS101-06704 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr11:2857650-2858890 |
SNPs | | Number: 3 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf12 | MA0742.1 | chr11:2858473-2858488 | GCTGTGGGCGTGGCC | - | 6.06 | | PLAG1 | MA0163.1 | chr11:2858075-2858089 | GGGGCCCTAGAGGG | + | 6.02 | | SP1 | MA0079.4 | chr11:2858475-2858490 | TGTGGGCGTGGCCAA | - | 7.26 | | SP3 | MA0746.2 | chr11:2858475-2858488 | TGTGGGCGTGGCC | - | 6.64 | | SP4 | MA0685.1 | chr11:2858473-2858490 | GCTGTGGGCGTGGCCAA | - | 6.7 | | SP8 | MA0747.1 | chr11:2858475-2858487 | TGTGGGCGTGGC | - | 6.22 |
|
| | 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 |
| GH11I002834 | chr11 | 2855938 | 2862214 |
|
Enhancer Sequence | GGGTGAGGCC GGACTGCACT CCAAGGGGAG GAGGTGGGAG AGCACAGCCT GGCTGCTGCC 60
ACCAAGCTCC CCAGAAGAGG GGACCCCTCC CCCCGAACAC CAGCACATGT AGGCAGAAAG 120
ACTTGGCCTG TGGAGCCCTC AGCCTCCACG CCCACCAGCA GGGACTGGGT GGTGATGTCA 180
GCAATCCCCA CAGAAAGGAG GGCTGCACAG CCGTCCCAGG AGCCAGCACT GTCCCCGTGA 240
TTCTACGTGC AGCCTCCACA AGTGTGTCGC ATGGAAACAA GCAGTGGAGA GCCACATGTG 300
TGTCACATCA CGCCTCGCCT CACTCGTGCT AAACCTCGCT GACCAGGCAG AACCAGGCAC 360
GAGCTGCGTA TCAAAGTTGC TGGAAGGAGA AACATCAGAT CCCTAAGCTG GTTACCTGGC 420
AGGCAGGGGC CCTAGAGGGA AATGGGGCAG GTGAAATGGA GATGTGTCTT TGAAATGTCT 480
TTATTTGGCG GGAGAACGTC TTCATAGGGT ACTTATACCA TGAAAAACCC TGTACACAGA 540
CTAATTTTGA AGCAAACATG TGAGGCGTTC ACAGAAAGGG TTCAGGAAGA CAAGCACCCC 600
AGCCGCAGAG AGCCCGTGGG CTGGGGGCAC GGGGCATGGC AGCCCTCTCC TGGGGATGGG 660
CAGGATGGGG CACGTAGGGC GGAGGAAGAG GCTCACATGG TGTGCGTGTT TGGGAGCACC 720
CTGGGCAGCC TCTCGAGTGT CCAGAGAGAG GACACCGTCT TGAGCCAGCA GGGACAGCCA 780
AGAGCGCCCG GGGAGAGGCC TGGGTGGAGA CAGAACACAG CAGGCTGTGG GCGTGGCCAA 840
TGTTGAGGGA CGGAGGTGGC CAGAGGCCTC TCAGTGGTGC CCAGGGAGCT GGGGACGAGG 900
GGCCTCATCC TTCCCCTGAG CCCCTCCCTT CAGGCCCAGG GAGTGGCCTG GGGCCCAGGA 960
GAGCCCGCTC CGCGCTCACA GCCTCCGTTC CCAGACACGC CCGGGCCTGA GCCCCCAGGC 1020
TGCACTGTGC CACAGAACAG ACTCCCCGGC CCCTCCCTGC TCGAGAGGTG ACCAAGGCCC 1080
AGGGTCTCCC AGCGAGCAAG AGGCCATTGA ACTGTTGTTG GCTGTGCAGT GCCCTGCCCT 1140
CGGGGAGGCG GCCTCTAAGA AGCACACACC ACCAGCAGGA ACCGGGCAGA CAGAGGTGGG 1200
GGATGGAAAG CAGGGGAAGT GGCCACAGCC AAACCAGGAG 1240
|
