| Tag | Content |
|---|
EnhancerAtlas ID | HS034-31298 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr9:139236880-139238020 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr9:139237513-139237532 | CACCGCCCTCTGCTGGCCC | - | 7.31 | | Klf12 | MA0742.1 | chr9:139237377-139237392 | GTTGTGGGCGTGGTC | - | 6.44 | | SP3 | MA0746.2 | chr9:139237379-139237392 | TGTGGGCGTGGTC | - | 6.21 | | SP3 | MA0746.2 | chr9:139237401-139237414 | GGTGGGCGTGGCA | - | 7.12 | | SP8 | MA0747.1 | chr9:139237401-139237413 | GGTGGGCGTGGC | - | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_49050 | chr9:139234769-139241356 | Right_Atrium |
|
| | 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 |
| GH09I136340 | chr9 | 139235197 | 139238747 |
|
Enhancer Sequence | CTCTGGCTCC TCTGTGCCGC CCCGAGTGCG GGACCCCTTC CAGCCGGCCG GACGCCTCCT 60
CCCCCAGGGC TGGGGAAGGG TCCTCCTCCC CGCCCAGGGC AGCCCGGCAG CCTGGCTGGG 120
GCCGCCGCCC GGCTGCCGCT GTGGGAGGCA GGCTGCACAC CTAGAGCCTG GGCGGCCCTG 180
GGTGAGACCC CGGCTCAGCT GAGCCTGGCA GGGACAGGGC CTTGAGGCCG GGAGTCTGGA 240
CCCGGCGTTG CGGGTTGGGG GCGCCACGGA AGGACCCACG CAGCCTCCCC ATTCGGCAGG 300
TGCGGAGGGC GGGGTGGATC TGCGAGCTGC GGGAGGGGAG GGGGGTGCAG AGCCGCGCTA 360
GAGCCTGGCC GTGCGGAGGG GGCGCCAGGG CTGGGGGCAC AGGAGGGCGC TGCCCAGCGG 420
GGTGTGGGCA GGGAGGAGGA AGTCGTCTGG AGGTGGGGCT TCAGCCCGGC GGGGACGCGG 480
TGGGGCGTGG CCTTGCTGTT GTGGGCGTGG TCCATGGGGG CGGTGGGCGT GGCAGAGGCT 540
GGTGGGTTTG GTGTCCCGTT GATAAACACA AGGAGACTTA CGTGCGGCTG GAGGACAAAG 600
AGCCTTGGCG CGGCTCAGTC AGCGTATTAA TCTCACCGCC CTCTGCTGGC CCCTCCCCAG 660
CCAGCAGAGA AGCCCCAGAA GTGTGTCTGG GGGTCACCAC CCTGCCAGCC ACTGCCCTTG 720
TCCAGCTCCT CTGGGTGTGT GGCCTCTATG AGACCCTGAC AGCAACCAGC CCCCACCTCC 780
CTGGCCAGAG GGCACAGGCC CGGGCCTCCC ACACTTGCTC CTGGGCTGCC CACCCCCCAC 840
CCCAGCAAGG GTGCCAGGCA GGACGGAGGC TCTGCTGCCA CTCTTGGTGC GGGCAGCATG 900
ATTGGCATGT TGGGAGGAGG GAGCCGGCCC TGAGCCCTGC AGGACCGCCC CCTGCCCTTG 960
GCCTGTCCCC GATGGCCCTG CCTGTCCCAC AGGATGTGCG ACTGCCCTCG GCCCTGCTGA 1020
CTGTACTTCT CAGCCCTCCA CCGTCTGGGC CCTGCTCAGG GCGTTGTGAG CACGGTACAC 1080
AAGAGTTACT GGGGGAGCAT GCCACCAGCC TTCCTGGGAG AAGTCCCCTG AACGTCCCAA 1140
|
