Chrom. | Start | End | Enhancer ID | TSS of gene | Distance between enhancer and TSS | Tissues that enhancer appears | More |
---|---|---|---|---|---|---|---|
chr12 | 49829845 | 49833995 | enh2332 | 49932940 | 98945 |
|
|
chr12 | 49843725 | 49847875 | enh103718 | 49932940 | 85065 |
|
|
chr12 | 49858565 | 49866455 | enh2333 | 49932940 | 66485 |
|
|
chr12 | 49866902 | 49867154 | vista13344 | 49932940 | 65786 |
|
|
chr12 | 49870694 | 49878366 | enh68137 | 49932940 | 54574 |
|
|
chr12 | 49894525 | 49903609 | enh29567 | 49932940 | 29331 |
|
|
chr12 | 49905171 | 49910869 | enh86106 | 49932940 | 22071 |
|
|
chr12 | 49923645 | 49927795 | enh109551 | 49932940 | 5145 |
|
|
chr12 | 49972294 | 49976620 | enh62263 | 49932940 | 39354 |
|
|
chr12 | 49972592 | 49972801 | vista13345 | 49932940 | 39652 |
|
|
chr12 | 49988265 | 49992415 | enh2334 | 49932940 | 55325 |
|
|
chr12 | 50007585 | 50024007 | enh29568 | 49932940 | 74645 |
|
|
chr12 | 50019010 | 50019299 | vista13346 | 49932940 | 86070 |
|
|
chr12 | 50019907 | 50020190 | vista13347 | 49932940 | 86967 |
|
|
chr12 | 50020601 | 50020960 | vista13348 | 49932940 | 87661 |
|
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 | 49368971 | rs11168814 | T | C | 563969 | Esophagus | 0.181501 | 2618795 | |
chr12 | 50043023 | rs144511742 | G | A | 90932 | Heart | 0.257583 | 2622250 | |
chr12 | 49703930 | rs75590517 | C | G | 229010 | Pancreas | 0.235465 | 2620581 | |
chr12 | 50333713 | rs11169219 | G | C | 381622 | Ovary | 0.0906618 | 2624228 |
Genomic Location | chr12:49932940-49952091[+] |
TSS | 49932940 |
Gene Name | KCNH3 |
Ensembl ID | ENSG00000135519.6 |
ENTREZID | 23416 |
Uniprot | |
Q9ULD8 | |
Protein Name | |
subfamily H | |
Potassium voltage-gated channel | |
Potassium voltage-gated channel subfamily H member 3 |