| Tag | Content |
|---|
EnhancerAtlas ID | HS037-41238 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr9:139236800-139237950 |
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 | TCCCGACGTT TTCTTTCTTG GAGCCAAGGA AAAGGGGGGC CGGAGTGGGA GGACGCTGGA 60
ACAATGCAGC TTCTGTCCCT CTCTGGCTCC TCTGTGCCGC CCCGAGTGCG GGACCCCTTC 120
CAGCCGGCCG GACGCCTCCT CCCCCAGGGC TGGGGAAGGG TCCTCCTCCC CGCCCAGGGC 180
AGCCCGGCAG CCTGGCTGGG GCCGCCGCCC GGCTGCCGCT GTGGGAGGCA GGCTGCACAC 240
CTAGAGCCTG GGCGGCCCTG GGTGAGACCC CGGCTCAGCT GAGCCTGGCA GGGACAGGGC 300
CTTGAGGCCG GGAGTCTGGA CCCGGCGTTG CGGGTTGGGG GCGCCACGGA AGGACCCACG 360
CAGCCTCCCC ATTCGGCAGG TGCGGAGGGC GGGGTGGATC TGCGAGCTGC GGGAGGGGAG 420
GGGGGTGCAG AGCCGCGCTA GAGCCTGGCC GTGCGGAGGG GGCGCCAGGG CTGGGGGCAC 480
AGGAGGGCGC TGCCCAGCGG GGTGTGGGCA GGGAGGAGGA AGTCGTCTGG AGGTGGGGCT 540
TCAGCCCGGC GGGGACGCGG TGGGGCGTGG CCTTGCTGTT GTGGGCGTGG TCCATGGGGG 600
CGGTGGGCGT GGCAGAGGCT GGTGGGTTTG GTGTCCCGTT GATAAACACA AGGAGACTTA 660
CGTGCGGCTG GAGGACAAAG AGCCTTGGCG CGGCTCAGTC AGCGTATTAA TCTCACCGCC 720
CTCTGCTGGC CCCTCCCCAG CCAGCAGAGA AGCCCCAGAA GTGTGTCTGG GGGTCACCAC 780
CCTGCCAGCC ACTGCCCTTG TCCAGCTCCT CTGGGTGTGT GGCCTCTATG AGACCCTGAC 840
AGCAACCAGC CCCCACCTCC CTGGCCAGAG GGCACAGGCC CGGGCCTCCC ACACTTGCTC 900
CTGGGCTGCC CACCCCCCAC CCCAGCAAGG GTGCCAGGCA GGACGGAGGC TCTGCTGCCA 960
CTCTTGGTGC GGGCAGCATG ATTGGCATGT TGGGAGGAGG GAGCCGGCCC TGAGCCCTGC 1020
AGGACCGCCC CCTGCCCTTG GCCTGTCCCC GATGGCCCTG CCTGTCCCAC AGGATGTGCG 1080
ACTGCCCTCG GCCCTGCTGA CTGTACTTCT CAGCCCTCCA CCGTCTGGGC CCTGCTCAGG 1140
GCGTTGTGAG 1150
|
