| Tag | Content |
|---|
EnhancerAtlas ID | HS062-06003 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr16:146590-147520 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr16:147056-147075 | TGCTGCCCCCTGGTGGCCA | - | 9.61 | | KLF14 | MA0740.1 | chr16:147166-147180 | GGCCACGCCCACAT | + | 6.74 | | Klf12 | MA0742.1 | chr16:147166-147181 | GGCCACGCCCACATG | + | 6.51 | | SP1 | MA0079.4 | chr16:147164-147179 | TGGGCCACGCCCACA | + | 6.01 | | SP3 | MA0746.2 | chr16:147166-147179 | GGCCACGCCCACA | + | 6.64 | | SP8 | MA0747.1 | chr16:147167-147179 | GCCACGCCCACA | + | 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 |
| GH16I000096 | chr16 | 146743 | 148011 |
|
Enhancer Sequence | TTGAGCCCAG GAGTATGAGG CCAGCCAGGG CAACATAGGG AAACCCCGTC TCTACCAAAA 60
AAAAAAAAAA AAAAAAAATA TTAGCCAGGC GCACACCTGT AGTCCCAGCT ACTTGGGAGG 120
ATGCTTGAGC CTGGGTGGAT CATGATGGCA CCACCACATG CCAGCCTGGG AGACAGAGCA 180
AGAACCTGTC TCAGAAAAGA AAAAAGAAAT ACAAGGGCAC AATTTGGTAA GTGCTCTCAC 240
AGAGGATAGA TAAAGGGTCC TGAGATACAG AGGCGGGAGA CTTACTCTCA AAGACAGAAT 300
CCAAAAAGGC TGCTTTCGGG GAAAAGTGGC CTGAGAGTCA GGCCTTGTTG GACAAGTTCC 360
CCTAACGTGC TAAGCAGAGA CCTGTTTCAC AGGCCAAAAG AGCATGGAAG CTCAGCCAGA 420
GGGACCCAGG CGGGCCCACC TCACGCCTGT GTTCCTCGGC AGCCTCTGCT GCCCCCTGGT 480
GGCCATGCTG TGCACACCGC CACCAGACGA GGGCGCCACC CACAGGCACC ACCTGCTCCC 540
ACCCTCAGGC AGTATTTCAA TGGTCCCGTG GCTCTGGGCC ACGCCCACAT GACTAGCAGC 600
CACAGCTGAT CCCATGGCCT GTTGGCCACC CCATCAGCAG CCCCTGCTTC TGATTTCTCC 660
CCGTGCTTTT TTTTTTTTTG GAAACAGAGT CGCCCAGGCT GGAGTACAGT GGCACAATCT 720
CAGCTAACTG CAACCTCTGC CTCCCAGGCT CAATTGATCC TCACACCTCA TACCCCCAAG 780
TAGCTGGGAC TACAGGTGCA CGCCACCACA CCCAGCTATT TTTTTTTTTT TTTTTTTTGT 840
ATTTTTTGTA GAGACGGGGT TTTGCCATGT TGCTCAGGCT GGTCTCAAAG TCCTGGGCTA 900
GGATGACAGG CATGAGCCAC CGTGCCCAGC 930
|
