| Chrom. | Start | End | Enhancer ID | TSS of gene | Distance between enhancer and TSS | Tissues that enhancer appears | More |
|---|---|---|---|---|---|---|---|
| chr6 | 42837351 | 42841695 | enh55755 | 42928496 | 86801 |
|
|
| chr6 | 42864621 | 42878115 | enh9129 | 42928496 | 50381 |
|
|
| chr6 | 42879334 | 42879417 | vista51996 | 42928496 | 49079 |
|
|
| chr6 | 42898508 | 42898648 | vista51997 | 42928496 | 29848 |
|
|
| chr6 | 42940985 | 42945135 | enh9130 | 42928496 | 12489 |
|
|
| chr6 | 42944082 | 42944413 | vista51998 | 42928496 | 15586 |
|
|
| chr6 | 42944777 | 42944970 | vista51999 | 42928496 | 16281 |
|
|
| chr6 | 42962325 | 42969267 | enh46127 | 42928496 | 33829 |
|
|
| chr6 | 42982951 | 42983183 | vista52000 | 42928496 | 54455 |
|
|
| chr6 | 43001164 | 43001472 | vista52001 | 42928496 | 72668 |
|
| 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 |
|---|---|---|---|---|---|---|---|---|---|
| chr6 | 42947013 | rs9462860 | G | A,C | 15395 | Esophagus | 0.149247 | 9035426 | |
| chr6 | 42896948 | rs562972889 | T | TCTC | 31548 | Stomach | 0.0295153 | 9035307 |
| Genomic Location | chr6:42928496-42931618[+] |
| TSS | 42928496 |
| Gene Name | GNMT |
| Ensembl ID | ENSG00000124713.5 |
| ENTREZID | 27232 |
| Uniprot | |
| V9HW60 | |
| Q14749 | |
| A0A0S2Z5F2 | |
| Protein Name | |
| Glycine N-methyltransferase | |
| Glycine N-methyltransferase isoform 3 | |
| Glycine N-methyltransferase isoform 4 |