| Chrom. | Start | End | Enhancer ID | TSS of gene | Distance between enhancer and TSS | Tissues that enhancer appears | More |
|---|---|---|---|---|---|---|---|
| chr17 | 56230515 | 56230722 | vista25278 | 56296966 | 66244 |
|
|
| chr17 | 56254125 | 56258275 | enh52538 | 56296966 | 38691 |
|
|
| chr17 | 56260825 | 56264975 | enh91172 | 56296966 | 31991 |
|
|
| chr17 | 56304259 | 56312813 | enh32244 | 56296966 | 7293 |
|
|
| chr17 | 56310140 | 56310517 | vista25279 | 56296966 | 13174 |
|
|
| chr17 | 56311025 | 56311130 | vista25280 | 56296966 | 14059 |
|
|
| chr17 | 56311784 | 56312133 | vista25281 | 56296966 | 14818 |
|
|
| chr17 | 56359005 | 56359460 | vista25282 | 56296966 | 62039 |
|
|
| chr17 | 56362029 | 56362418 | vista25283 | 56296966 | 65063 |
|
|
| chr17 | 56391648 | 56391970 | vista25284 | 56296966 | 94682 |
|
| 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 |
|---|---|---|---|---|---|---|---|---|---|
| chr17 | 55613009 | rs17834539 | C | T | 669794 | Esophagus | 0.0612972 | 4950849 | |
| chr17 | 55620229 | rs9906675 | C | T | 662574 | Heart | 0.344119 | 4950963 | |
| chr17 | 55308030 | rs148271263 | C | T | 974773 | Breast | 0.280578 | 4947878 | |
| chr17 | 56416338 | rs117356097 | C | T | 119372 | Spleen | 0.453203 | 4956010 | |
| chr17 | 55737663 | rs79439437 | C | T | 545140 | Ovary | 0.342328 | 4952243 |
| Genomic Location | chr17:56282803-56296966[-] |
| TSS | 56296966 |
| Gene Name | MKS1 |
| Ensembl ID | ENSG00000011143.12 |
| ENTREZID | 54903 |
| Uniprot | |
| A0A0S2Z5Z2 | |
| H0Y2S2 | |
| B4DVC5 | |
| Q9NXB0 | |
| Protein Name | |
| Meckel syndrome type 1 isoform 1 | |
| Meckel syndrome type 1 isoform 2 | |
| Meckel syndrome type 1 isoform 3 | |
| Meckel syndrome type 1 protein |