| Chrom. | Start | End | Enhancer ID | TSS of gene | Distance between enhancer and TSS | Tissues that enhancer appears | More |
|---|---|---|---|---|---|---|---|
| chr12 | 48494905 | 48499055 | enh2324 | 48592170 | 93115 |
|
|
| chr12 | 48567565 | 48572175 | enh68135 | 48592170 | 19995 |
|
|
| chr12 | 48579978 | 48580344 | vista13311 | 48592170 | 11826 |
|
|
| chr12 | 48581324 | 48585664 | enh102463 | 48592170 | 6506 |
|
|
| chr12 | 48604625 | 48608775 | enh98960 | 48592170 | 12455 |
|
|
| chr12 | 48629085 | 48633235 | enh110543 | 48592170 | 36915 |
|
|
| chr12 | 48657645 | 48663335 | enh75033 | 48592170 | 65475 |
|
|
| chr12 | 48677925 | 48682695 | enh96294 | 48592170 | 85755 |
|
|
| chr12 | 48683365 | 48688055 | enh96295 | 48592170 | 91195 |
|
|
| chr12 | 48688366 | 48693035 | enh98961 | 48592170 | 96196 |
|
| 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 |
|---|---|---|---|---|---|---|---|---|---|
| chr12 | 48582973 | rs10875764 | T | C | 9197 | Esophagus | 1.22266e-05 | 2616125 | |
| chr12 | 48588936 | rs11168450 | A | G | 3234 | Esophagus | 0.00362815 | 2616179 | |
| chr12 | 48195069 | rs3759407 | G | A | 397101 | Esophagus | 0.0961618 | 2613881 | |
| chr12 | 47811205 | rs2698792 | C | T | 780965 | Heart | 0.34072 | 2612299 | |
| chr12 | 48589462 | rs66507954 | T | C | 2708 | Thyroid | 4.75678e-13 | 2616186 | |
| chr12 | 48775885 | rs145473433 | A | G | 180071 | Adrenal | 0.238928 | 2616783 |
| Genomic Location | chr12:48592170-48595814[+] |
| TSS | 48592170 |
| Gene Name | DKFZP779L1853 |
| Ensembl ID | ENSG00000269514.1 |
| ENTREZID | 643162 |
| Uniprot | |
| Protein Name | |
| Putative uncharacterized protein DKFZp779L1853 |