Chrom. | Start | End | Enhancer ID | TSS of gene | Distance between enhancer and TSS | Tissues that enhancer appears | More |
---|---|---|---|---|---|---|---|
chr16 | 80963905 | 80974791 | enh16828 | 81069452 | 94661 |
|
|
chr16 | 80971971 | 80972227 | vista23114 | 81069452 | 97225 |
|
|
chr16 | 80979985 | 80984995 | enh81154 | 81069452 | 84457 |
|
|
chr16 | 81017255 | 81021455 | enh69197 | 81069452 | 47997 |
|
|
chr16 | 81024985 | 81030455 | enh16829 | 81069452 | 38997 |
|
|
chr16 | 81026963 | 81027197 | vista23115 | 81069452 | 42255 |
|
|
chr16 | 81038389 | 81038511 | vista23116 | 81069452 | 30941 |
|
|
chr16 | 81103485 | 81109411 | enh16830 | 81069452 | 34033 |
|
|
chr16 | 81137725 | 81143455 | enh16831 | 81069452 | 68273 |
|
|
chr16 | 81153365 | 81162915 | enh16832 | 81069452 | 83913 |
|
|
chr16 | 81166265 | 81182215 | enh16833 | 81069452 | 96813 |
|
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 | 81208788 | rs935930 | C | G,T | 127825 | Esophagus | 0.222517 | 4579951 | |
chr16 | 81907794 | rs9922366 | A | T | 826831 | Esophagus | 0.312444 | 4589529 | |
chr16 | 81223646 | rs8046301 | G | A | 142683 | Breast | 0.208448 | 4580316 | |
chr16 | 81140526 | rs11150340 | T | C | 59563 | Thyroid | 6.7668e-08 | 4578937 | |
chr16 | 81206400 | rs1377462 | C | T | 125437 | Stomach | 0.418979 | 4579852 | |
chr16 | 81669927 | rs186979692 | C | T | 588964 | Adrenal | 0.589408 | 4585820 |
Genomic Location | chr16:81069452-81080963[+] |
TSS | 81069452 |
Gene Name | ATMIN |
Ensembl ID | ENSG00000166454.5 |
ENTREZID | 23300 |
Uniprot | |
O43313 | |
Protein Name | |
ATM interactor |