Variant report
Variant | rs16950652 |
---|---|
Chromosome Location | chr18:44810442-44810443 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:3)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
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No data |
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Variant related genes | Relation type |
---|---|
ENSG00000267761 | TF binding region |
rs_ID | r2[population] |
---|---|
rs1347340 | 1.00[CEU][hapmap];0.86[EUR][1000 genomes] |
rs1347343 | 0.81[AFR][1000 genomes] |
rs16950644 | 0.96[YRI][hapmap];1.00[AFR][1000 genomes];0.91[ASN][1000 genomes] |
rs16950662 | 0.92[EUR][1000 genomes] |
rs16950692 | 0.98[AFR][1000 genomes];0.91[ASN][1000 genomes] |
rs16950719 | 0.92[EUR][1000 genomes] |
rs16950736 | 0.92[EUR][1000 genomes] |
rs16950741 | 0.92[EUR][1000 genomes] |
rs16950744 | 1.00[CEU][hapmap];0.92[EUR][1000 genomes] |
rs16950754 | 1.00[CEU][hapmap];0.92[EUR][1000 genomes] |
rs16950767 | 1.00[CEU][hapmap];0.92[EUR][1000 genomes] |
rs16950777 | 0.92[EUR][1000 genomes] |
rs1944287 | 0.98[AFR][1000 genomes];0.91[ASN][1000 genomes] |
rs28401248 | 0.86[ASN][1000 genomes] |
rs28455576 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28737231 | 0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs55687418 | 0.92[EUR][1000 genomes] |
rs55698938 | 0.92[EUR][1000 genomes] |
rs55704228 | 0.92[EUR][1000 genomes] |
rs55813572 | 0.92[EUR][1000 genomes] |
rs55825078 | 0.84[EUR][1000 genomes] |
rs55892143 | 0.92[EUR][1000 genomes] |
rs55977647 | 0.92[EUR][1000 genomes] |
rs56014831 | 0.92[EUR][1000 genomes] |
rs56077098 | 0.92[EUR][1000 genomes] |
rs56109704 | 0.92[EUR][1000 genomes] |
rs56287570 | 0.84[EUR][1000 genomes] |
rs58684150 | 0.92[EUR][1000 genomes] |
rs66485937 | 0.92[EUR][1000 genomes] |
rs66914705 | 0.92[EUR][1000 genomes] |
rs67119810 | 0.92[EUR][1000 genomes] |
rs67123015 | 0.92[EUR][1000 genomes] |
rs67514853 | 0.92[EUR][1000 genomes] |
rs67822267 | 0.92[EUR][1000 genomes] |
rs7241169 | 1.00[AFR][1000 genomes];0.86[ASN][1000 genomes] |
rs72906489 | 0.92[EUR][1000 genomes] |
rs72906494 | 0.92[EUR][1000 genomes] |
rs72906498 | 0.92[EUR][1000 genomes] |
rs72908505 | 0.92[EUR][1000 genomes] |
rs72908507 | 0.92[EUR][1000 genomes] |
rs72908508 | 0.92[EUR][1000 genomes] |
rs72908518 | 0.92[EUR][1000 genomes] |
rs72908529 | 0.92[EUR][1000 genomes] |
rs72908533 | 0.92[EUR][1000 genomes] |
rs72908537 | 0.92[EUR][1000 genomes] |
rs72908538 | 0.92[EUR][1000 genomes] |
rs72908542 | 0.92[EUR][1000 genomes] |
rs72908558 | 0.92[EUR][1000 genomes] |
rs72908572 | 0.92[EUR][1000 genomes] |
rs72908575 | 0.92[EUR][1000 genomes] |
rs72908588 | 0.85[EUR][1000 genomes] |
rs72910504 | 0.92[EUR][1000 genomes] |
rs72910505 | 0.92[EUR][1000 genomes] |
rs72910507 | 0.92[EUR][1000 genomes] |
rs72910512 | 0.92[EUR][1000 genomes] |
rs72910513 | 0.92[EUR][1000 genomes] |
rs72910516 | 0.92[EUR][1000 genomes] |
rs72910538 | 0.84[EUR][1000 genomes] |
rs72910540 | 0.84[EUR][1000 genomes] |
rs72910544 | 0.84[EUR][1000 genomes] |
rs72910547 | 0.84[EUR][1000 genomes] |
rs72910552 | 0.84[EUR][1000 genomes] |
rs72910554 | 0.84[EUR][1000 genomes] |
rs72912419 | 0.84[EUR][1000 genomes] |
rs72912427 | 0.84[EUR][1000 genomes] |
rs72912445 | 0.84[EUR][1000 genomes] |
rs72912456 | 0.84[EUR][1000 genomes] |
rs72912458 | 0.84[EUR][1000 genomes] |
rs72912473 | 0.84[EUR][1000 genomes] |
rs72914847 | 0.92[EUR][1000 genomes] |
rs72914848 | 0.92[EUR][1000 genomes] |
rs72914856 | 0.92[EUR][1000 genomes] |
rs72914857 | 0.92[EUR][1000 genomes] |
rs72914862 | 0.92[EUR][1000 genomes] |
rs8087053 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs8099226 | 0.97[AFR][1000 genomes];0.91[ASN][1000 genomes] |
rs9946349 | 0.91[ASN][1000 genomes] |
rs9949210 | 0.86[ASN][1000 genomes] |
rs9950003 | 0.91[ASN][1000 genomes] |
rs9950055 | 0.91[ASN][1000 genomes] |
rs9952842 | 0.91[ASN][1000 genomes] |
rs9956537 | 0.86[ASN][1000 genomes] |
rs9959416 | 0.86[ASN][1000 genomes] |
rs9962170 | 1.00[CHB][hapmap];0.91[ASN][1000 genomes] |
rs9964499 | 0.91[ASN][1000 genomes] |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr18:44810400-44819200 | Weak transcription | Muscle Satellite Cultured Cells | -- |