Chrom. | Start | End | Enhancer ID | TSS of gene | Distance between enhancer and TSS | Tissues that enhancer appears | More |
---|---|---|---|---|---|---|---|
chr15 | 41300665 | 41313040 | enh16074 | 41408552 | 95512 |
|
|
chr15 | 41325205 | 41330535 | enh51980 | 41408552 | 78017 |
|
|
chr15 | 41394525 | 41398753 | enh80967 | 41408552 | 9799 |
|
|
chr15 | 41414365 | 41420735 | enh92581 | 41408552 | 5813 |
|
|
chr15 | 41429268 | 41437870 | enh58636 | 41408552 | 20716 |
|
|
chr15 | 41441045 | 41448835 | enh80968 | 41408552 | 32493 |
|
|
chr15 | 41451305 | 41457589 | enh31325 | 41408552 | 42753 |
|
|
chr15 | 41456018 | 41456111 | vista19753 | 41408552 | 47466 |
|
Chrom. | Start | End | TF name | Source | Predicted site? | Tissue | TSS of gene | Distance between TFBS and gene | id | More |
---|
Chrom. | Position | dbSNP ID | Reference Allele | Alternative Allele | Distance between TSS and SNP | Tissue | q Value | id | More |
---|---|---|---|---|---|---|---|---|---|
chr15 | 42264135 | rs118054745 | C | T | 855583 | Esophagus | 0.179936 | 3920294 | |
chr15 | 40847008 | rs2278887 | C | T | 424070 | Esophagus | 0.256025 | 3913164 | |
chr15 | 40807881 | rs74011171 | T | C | 463197 | Esophagus | 0.014535 | 3912916 | |
chr15 | 42233055 | rs117595127 | G | C | 824503 | Heart | 0.0664649 | 3919948 | |
chr15 | 41258121 | rs143569302 | C | T | 12957 | Pancreas | 0.102715 | 3915600 | |
chr15 | 41989091 | rs61736074 | C | A | 580539 | Ovary | 0.718261 | 3918906 | |
chr15 | 40928153 | rs147325866 | G | C | 342925 | Stomach | 0.43726 | 3913578 | |
chr15 | 41194334 | rs146015565 | G | A | 76744 | Adrenal | 0.256112 | 3914954 |
Genomic Location | chr15:41271078-41408552[-] |
TSS | 41408552 |
Gene Name | INO80 |
Ensembl ID | ENSG00000128908.11 |
ENTREZID | 54617 |
Uniprot | |
Q9ULG1 | |
A0A024R9R7 | |
Protein Name | |
DNA helicase INO80 |