Variant report
Variant | rs56053392 |
---|---|
Chromosome Location | chr5:35764835-35764836 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10041865 | 1.00[EUR][1000 genomes] |
rs10058723 | 1.00[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs10077553 | 1.00[EUR][1000 genomes] |
rs10079269 | 1.00[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs10079517 | 1.00[EUR][1000 genomes] |
rs10491432 | 1.00[EUR][1000 genomes] |
rs10491433 | 1.00[EUR][1000 genomes] |
rs11567717 | 1.00[EUR][1000 genomes] |
rs11567730 | 1.00[EUR][1000 genomes] |
rs11567764 | 1.00[EUR][1000 genomes] |
rs11951270 | 1.00[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs11954459 | 0.81[ASN][1000 genomes] |
rs11954524 | 0.81[ASN][1000 genomes] |
rs11958548 | 0.90[ASN][1000 genomes] |
rs1374015 | 1.00[EUR][1000 genomes] |
rs1494570 | 1.00[EUR][1000 genomes] |
rs16902367 | 1.00[EUR][1000 genomes] |
rs16902514 | 1.00[EUR][1000 genomes] |
rs16902535 | 1.00[EUR][1000 genomes] |
rs16902557 | 1.00[EUR][1000 genomes] |
rs16902562 | 1.00[EUR][1000 genomes] |
rs16902592 | 1.00[EUR][1000 genomes] |
rs16902593 | 1.00[EUR][1000 genomes] |
rs16902594 | 1.00[EUR][1000 genomes] |
rs16902638 | 1.00[EUR][1000 genomes] |
rs16902639 | 1.00[EUR][1000 genomes] |
rs16902643 | 1.00[EUR][1000 genomes] |
rs2277044 | 0.81[ASN][1000 genomes] |
rs28756345 | 1.00[EUR][1000 genomes] |
rs55662701 | 1.00[EUR][1000 genomes] |
rs55696459 | 1.00[EUR][1000 genomes] |
rs56169453 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs56276485 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs56297110 | 1.00[EUR][1000 genomes] |
rs56773364 | 1.00[EUR][1000 genomes] |
rs57116204 | 0.81[ASN][1000 genomes] |
rs57435143 | 1.00[EUR][1000 genomes] |
rs57498894 | 1.00[EUR][1000 genomes] |
rs57681685 | 0.81[ASN][1000 genomes] |
rs58390944 | 0.90[ASN][1000 genomes] |
rs58522285 | 0.81[ASN][1000 genomes] |
rs58541693 | 1.00[EUR][1000 genomes] |
rs58671818 | 1.00[EUR][1000 genomes] |
rs58846527 | 0.81[ASN][1000 genomes] |
rs58872016 | 1.00[EUR][1000 genomes] |
rs59555387 | 1.00[EUR][1000 genomes] |
rs59714026 | 1.00[EUR][1000 genomes] |
rs60501022 | 0.81[ASN][1000 genomes] |
rs61180877 | 0.81[ASN][1000 genomes] |
rs61373681 | 0.81[ASN][1000 genomes] |
rs6451222 | 1.00[EUR][1000 genomes] |
rs6861184 | 1.00[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs6864736 | 1.00[EUR][1000 genomes] |
rs6875303 | 1.00[EUR][1000 genomes] |
rs6876261 | 1.00[EUR][1000 genomes] |
rs6881747 | 1.00[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs6881919 | 1.00[EUR][1000 genomes] |
rs6894309 | 1.00[EUR][1000 genomes] |
rs73076116 | 1.00[EUR][1000 genomes] |
rs73080218 | 1.00[EUR][1000 genomes] |
rs73080241 | 1.00[EUR][1000 genomes] |
rs73080293 | 1.00[EUR][1000 genomes] |
rs73082265 | 1.00[EUR][1000 genomes] |
rs73082277 | 1.00[EUR][1000 genomes] |
rs73084351 | 1.00[EUR][1000 genomes] |
rs73084388 | 1.00[EUR][1000 genomes] |
rs73084398 | 1.00[EUR][1000 genomes] |
rs73086208 | 1.00[EUR][1000 genomes] |
rs73086212 | 1.00[EUR][1000 genomes] |
rs73086213 | 1.00[EUR][1000 genomes] |
rs73086237 | 1.00[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs73086243 | 1.00[EUR][1000 genomes] |
rs73086251 | 0.90[AFR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs73086255 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs73086261 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs73086281 | 1.00[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs73086282 | 1.00[EUR][1000 genomes] |
rs73086302 | 1.00[EUR][1000 genomes] |
rs73088209 | 1.00[EUR][1000 genomes] |
rs73088244 | 1.00[EUR][1000 genomes] |
rs73090209 | 1.00[EUR][1000 genomes] |
rs73090222 | 1.00[EUR][1000 genomes] |
rs73090239 | 1.00[EUR][1000 genomes] |
rs73090241 | 1.00[EUR][1000 genomes] |
rs73090248 | 1.00[EUR][1000 genomes] |
rs73090257 | 1.00[EUR][1000 genomes] |
rs73090276 | 1.00[EUR][1000 genomes] |
rs73090284 | 1.00[EUR][1000 genomes] |
rs73090289 | 1.00[EUR][1000 genomes] |
rs73090291 | 1.00[EUR][1000 genomes] |
rs73090295 | 1.00[EUR][1000 genomes] |
rs73090298 | 1.00[EUR][1000 genomes] |
rs73092011 | 1.00[EUR][1000 genomes] |
rs73092033 | 1.00[EUR][1000 genomes] |
rs73092034 | 1.00[EUR][1000 genomes] |
rs73092092 | 1.00[EUR][1000 genomes] |
rs73092100 | 1.00[EUR][1000 genomes] |
rs73094009 | 1.00[EUR][1000 genomes] |
rs73094019 | 1.00[EUR][1000 genomes] |
rs73094022 | 1.00[EUR][1000 genomes] |
rs73747933 | 0.90[ASN][1000 genomes] |
rs73747964 | 0.81[ASN][1000 genomes] |
rs73747965 | 0.81[ASN][1000 genomes] |
rs73747966 | 0.81[ASN][1000 genomes] |
rs73747969 | 0.81[ASN][1000 genomes] |
rs73747970 | 0.81[ASN][1000 genomes] |
rs73747971 | 0.81[ASN][1000 genomes] |
rs73747973 | 0.81[ASN][1000 genomes] |
rs73747974 | 0.81[ASN][1000 genomes] |
rs73747977 | 0.81[ASN][1000 genomes] |
rs73747978 | 0.81[ASN][1000 genomes] |
rs73750806 | 1.00[EUR][1000 genomes] |
rs73750816 | 1.00[EUR][1000 genomes] |
rs73750817 | 1.00[EUR][1000 genomes] |
rs7700501 | 0.81[ASN][1000 genomes] |
rs7700688 | 0.81[ASN][1000 genomes] |
rs7701519 | 1.00[EUR][1000 genomes] |
rs7704710 | 1.00[EUR][1000 genomes] |
rs7708334 | 1.00[EUR][1000 genomes] |
rs7710405 | 1.00[EUR][1000 genomes] |
rs7714297 | 1.00[EUR][1000 genomes] |
rs7720394 | 1.00[EUR][1000 genomes] |
rs7724777 | 1.00[EUR][1000 genomes] |
rs9292610 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv525477 | chr5:35530905-35792990 | Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:35763000-35766200 | Weak transcription | Osteobl | bone |
2 | chr5:35764800-35767000 | Enhancers | Hela-S3 | cervix |