| Chrom. | Start | End | Enhancer ID | TSS of gene | Distance between enhancer and TSS | Tissues that enhancer appears | More |
|---|---|---|---|---|---|---|---|
| chr16 | 83094 | 91675 | enh3839 | 69452 | 13642 |
|
|
| chr16 | 85163 | 85424 | vista21496 | 69452 | 15711 |
|
|
| chr16 | 115405 | 125035 | enh99305 | 69452 | 45953 |
|
|
| chr16 | 121563 | 121849 | vista21497 | 69452 | 52111 |
|
|
| chr16 | 124533 | 124922 | vista21498 | 69452 | 55081 |
|
|
| chr16 | 127789 | 133393 | enh102537 | 69452 | 58337 |
|
|
| chr16 | 130955 | 131250 | vista21499 | 69452 | 61503 |
|
|
| chr16 | 145023 | 145249 | vista21500 | 69452 | 75571 |
|
|
| chr16 | 150045 | 161355 | enh64930 | 69452 | 80593 |
|
|
| chr16 | 151121 | 151408 | vista21501 | 69452 | 81669 |
|
|
| chr16 | 154913 | 155267 | vista21502 | 69452 | 85461 |
|
|
| chr16 | 163381 | 163878 | vista21503 | 69452 | 93929 |
|
| 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 |
|---|---|---|---|---|---|---|---|---|---|
| chr16 | 144428 | rs34769159 | A | G | 74976 | Esophagus | 0.100635 | 4244173 | |
| chr16 | 379379 | rs60769452 | G | A | 309927 | Heart | 0.182204 | 4245270 | |
| chr16 | 733572 | rs187664088 | C | T | 664120 | Pancreas | 0.211382 | 4248243 | |
| chr16 | 640440 | rs61753371 | C | T | 570988 | Thyroid | 0.112002 | 4247359 | |
| chr16 | 867594 | rs12325200 | C | T | 798142 | Stomach | 0.336133 | 4249593 |
| Genomic Location | chr16:64043-69452[-] |
| TSS | 69452 |
| Gene Name | WASH4P |
| Ensembl ID | ENSG00000234769.4 |
| ENTREZID | 374677 |
| Uniprot | |
| Protein Name | |
| Putative WAS protein family homolog 4 |