Chrom. | Start | End | Enhancer ID | TSS of gene | Distance between enhancer and TSS | Tissues that enhancer appears | More |
---|---|---|---|---|---|---|---|
chr16 | 756470 | 756692 | vista21523 | 838046 | 81354 |
|
|
chr16 | 767105 | 774255 | enh3840 | 838046 | 63791 |
|
|
chr16 | 776285 | 786915 | enh3841 | 838046 | 51131 |
|
|
chr16 | 797185 | 802775 | enh16492 | 838046 | 35271 |
|
|
chr16 | 802051 | 802260 | vista21524 | 838046 | 35786 |
|
|
chr16 | 809662 | 809847 | vista21525 | 838046 | 28199 |
|
|
chr16 | 858833 | 859023 | vista21526 | 838046 | 20787 |
|
|
chr16 | 861479 | 871615 | enh47913 | 838046 | 23433 |
|
|
chr16 | 873405 | 877775 | enh95490 | 838046 | 35359 |
|
|
chr16 | 880105 | 884995 | enh52188 | 838046 | 42059 |
|
|
chr16 | 890265 | 894475 | enh75741 | 838046 | 52219 |
|
|
chr16 | 891857 | 892147 | vista21527 | 838046 | 53811 |
|
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 | 839027 | rs2277902 | C | T | 0 | Esophagus | 0.260866 | 4249372 | |
chr16 | 1157152 | rs563906665 | G | C | 306415 | Esophagus | 0.24285 | 4252949 | |
chr16 | 1428483 | rs78229198 | C | T | 577746 | Heart | 0.0798419 | 4255984 | |
chr16 | 672470 | rs200405053 | AGC | A | 165576 | Spleen | 0.275184 | 4247788 | |
chr16 | 655652 | rs74000866 | G | A | 182394 | Liver | 0.0645729 | 4247617 | |
chr16 | 1236357 | rs150093639 | G | A | 385620 | Adrenal | 0.40056 | 4254442 |
Genomic Location | chr16:838046-850737[+] |
TSS | 838046 |
Gene Name | CHTF18 |
Ensembl ID | ENSG00000127586.12 |
ENTREZID | 63922 |
Uniprot | |
Q8WVB6 | |
Protein Name | |
Chromosome transmission fidelity protein 18 homolog |