Variant report
Variant | rs11004275 |
---|---|
Chromosome Location | chr10:56152840-56152841 |
allele | A/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] |
---|---|
rs10509011 | 0.86[CEU][hapmap] |
rs10740579 | 0.86[CEU][hapmap] |
rs10825306 | 0.86[CEU][hapmap] |
rs10825307 | 0.84[CEU][hapmap] |
rs10825319 | 0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11004239 | 0.86[CEU][hapmap] |
rs11004267 | 0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs11004270 | 0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs11004276 | 0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs1156657 | 0.86[CEU][hapmap] |
rs1159865 | 0.86[CEU][hapmap] |
rs1219862 | 1.00[YRI][hapmap] |
rs12354432 | 0.86[CEU][hapmap] |
rs1319836 | 0.86[CEU][hapmap] |
rs1342281 | 0.86[CEU][hapmap] |
rs1342285 | 0.86[CEU][hapmap] |
rs1342292 | 0.86[CEU][hapmap] |
rs1342294 | 0.81[CEU][hapmap] |
rs1342300 | 0.86[CEU][hapmap] |
rs1342305 | 0.86[CEU][hapmap] |
rs1418374 | 0.86[CEU][hapmap] |
rs1758816 | 0.82[CHB][hapmap] |
rs1935468 | 0.86[CEU][hapmap] |
rs1970519 | 0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap] |
rs1975405 | 0.84[CHB][hapmap] |
rs2028440 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs2050999 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs2078091 | 0.85[CHB][hapmap] |
rs2384424 | 0.85[CHB][hapmap] |
rs2384425 | 0.83[CHB][hapmap] |
rs4269840 | 0.90[CEU][hapmap] |
rs4411207 | 0.86[CEU][hapmap] |
rs4471336 | 0.86[CEU][hapmap] |
rs7073678 | 0.84[CHB][hapmap] |
rs7078666 | 0.89[CEU][hapmap] |
rs7087862 | 0.83[CHB][hapmap] |
rs7092744 | 0.81[CHB][hapmap] |
rs7342027 | 0.86[CEU][hapmap] |
rs7476422 | 0.82[CEU][hapmap] |
rs7918002 | 0.84[CEU][hapmap] |
rs7919725 | 0.86[CEU][hapmap] |
rs857368 | 0.82[CEU][hapmap] |
rs857371 | 0.86[CEU][hapmap] |
rs857373 | 0.86[CEU][hapmap] |
rs857374 | 0.86[CEU][hapmap] |
rs857392 | 0.85[CEU][hapmap] |
rs857394 | 0.86[CEU][hapmap] |
rs857395 | 0.86[CEU][hapmap] |
rs865091 | 0.81[CEU][hapmap] |
rs965265 | 0.86[CEU][hapmap] |
rs965266 | 0.86[CEU][hapmap] |
rs965267 | 0.90[CEU][hapmap] |
rs978842 | 0.86[CEU][hapmap] |
rs9943342 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1054364 | chr10:55925471-56196447 | ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
2 | nsv540633 | chr10:55925471-56196447 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | esv2753511 | chr10:56022197-56153636 | Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv1044020 | chr10:56038546-56224736 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
5 | nsv540634 | chr10:56038546-56224736 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
6 | nsv831879 | chr10:56059973-56210729 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
7 | nsv1052386 | chr10:56075990-56273476 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |