Variant report
Variant | rs61897479 |
---|---|
Chromosome Location | chr11:55638666-55638667 |
allele | C/G |
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] |
---|---|
rs12099295 | 0.86[EUR][1000 genomes] |
rs17510876 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs17511051 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs17514608 | 0.89[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs17527401 | 0.86[EUR][1000 genomes] |
rs17527710 | 0.85[EUR][1000 genomes] |
rs17527788 | 0.86[EUR][1000 genomes] |
rs17527850 | 0.86[EUR][1000 genomes] |
rs17527864 | 0.86[EUR][1000 genomes] |
rs17595801 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs17596694 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs17597646 | 0.87[EUR][1000 genomes] |
rs17598017 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs17598045 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs17598094 | 0.87[EUR][1000 genomes] |
rs17599457 | 0.86[EUR][1000 genomes] |
rs17599471 | 0.86[EUR][1000 genomes] |
rs17599899 | 0.86[EUR][1000 genomes] |
rs17599913 | 0.86[EUR][1000 genomes] |
rs17600692 | 0.83[EUR][1000 genomes] |
rs17600784 | 0.83[EUR][1000 genomes] |
rs17600820 | 0.83[EUR][1000 genomes] |
rs5018553 | 0.86[EUR][1000 genomes] |
rs55797579 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55833459 | 0.86[EUR][1000 genomes] |
rs55833816 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs56116804 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs56176720 | 0.86[EUR][1000 genomes] |
rs56178210 | 0.86[EUR][1000 genomes] |
rs56301431 | 0.89[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs56370444 | 0.86[EUR][1000 genomes] |
rs56402650 | 0.85[EUR][1000 genomes] |
rs61888468 | 0.83[EUR][1000 genomes] |
rs61888469 | 0.83[EUR][1000 genomes] |
rs61888470 | 0.89[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs61888471 | 0.83[EUR][1000 genomes] |
rs61888472 | 0.83[EUR][1000 genomes] |
rs61888473 | 0.83[EUR][1000 genomes] |
rs61888545 | 0.83[EUR][1000 genomes] |
rs61888546 | 0.83[EUR][1000 genomes] |
rs61889973 | 0.83[EUR][1000 genomes] |
rs61894170 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs61894171 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs61894172 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs61894173 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs61894174 | 0.87[EUR][1000 genomes] |
rs61894176 | 0.87[EUR][1000 genomes] |
rs61894198 | 0.87[EUR][1000 genomes] |
rs61894199 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs61894201 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs61894202 | 0.87[EUR][1000 genomes] |
rs61894203 | 0.87[EUR][1000 genomes] |
rs61894213 | 0.84[EUR][1000 genomes] |
rs61894214 | 0.84[EUR][1000 genomes] |
rs61894215 | 0.84[EUR][1000 genomes] |
rs61894216 | 0.83[EUR][1000 genomes] |
rs61895181 | 0.86[EUR][1000 genomes] |
rs61895182 | 0.86[EUR][1000 genomes] |
rs61895183 | 0.86[EUR][1000 genomes] |
rs61895184 | 0.86[EUR][1000 genomes] |
rs61895240 | 0.86[EUR][1000 genomes] |
rs61895241 | 0.86[EUR][1000 genomes] |
rs61895243 | 0.86[EUR][1000 genomes] |
rs61895244 | 0.86[EUR][1000 genomes] |
rs61895245 | 0.86[EUR][1000 genomes] |
rs61895246 | 0.86[EUR][1000 genomes] |
rs61895247 | 0.86[EUR][1000 genomes] |
rs61895248 | 0.86[EUR][1000 genomes] |
rs61895249 | 0.86[EUR][1000 genomes] |
rs61895250 | 0.89[AMR][1000 genomes] |
rs61895251 | 0.86[EUR][1000 genomes] |
rs61895252 | 0.86[EUR][1000 genomes] |
rs61895253 | 0.86[EUR][1000 genomes] |
rs61895254 | 0.86[EUR][1000 genomes] |
rs61895255 | 0.86[EUR][1000 genomes] |
rs61895256 | 0.86[EUR][1000 genomes] |
rs61895257 | 0.86[EUR][1000 genomes] |
rs61895258 | 0.86[EUR][1000 genomes] |
rs61895259 | 0.86[EUR][1000 genomes] |
rs61896168 | 0.86[EUR][1000 genomes] |
rs61896169 | 0.86[EUR][1000 genomes] |
rs61896182 | 0.86[EUR][1000 genomes] |
rs61896183 | 0.86[EUR][1000 genomes] |
rs61896184 | 0.86[EUR][1000 genomes] |
rs61896235 | 0.86[EUR][1000 genomes] |
rs61896236 | 0.85[EUR][1000 genomes] |
rs61896237 | 0.86[EUR][1000 genomes] |
rs61896238 | 0.86[EUR][1000 genomes] |
rs61896240 | 0.86[EUR][1000 genomes] |
rs61896241 | 0.86[EUR][1000 genomes] |
rs61896242 | 0.89[AMR][1000 genomes] |
rs61896244 | 0.86[EUR][1000 genomes] |
rs61896245 | 0.86[EUR][1000 genomes] |
rs61896247 | 0.86[EUR][1000 genomes] |
rs61896248 | 0.86[EUR][1000 genomes] |
rs61896249 | 0.86[EUR][1000 genomes] |
rs61896250 | 0.86[EUR][1000 genomes] |
rs61896251 | 0.86[EUR][1000 genomes] |
rs61896253 | 0.86[EUR][1000 genomes] |
rs61896254 | 0.86[EUR][1000 genomes] |
rs61896255 | 0.86[EUR][1000 genomes] |
rs61896256 | 0.86[EUR][1000 genomes] |
rs61896257 | 0.86[EUR][1000 genomes] |
rs61896258 | 0.86[EUR][1000 genomes] |
rs61896259 | 0.89[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs61896960 | 0.86[EUR][1000 genomes] |
rs61896961 | 0.86[EUR][1000 genomes] |
rs61896962 | 0.86[EUR][1000 genomes] |
rs61896963 | 0.86[EUR][1000 genomes] |
rs61896964 | 0.86[EUR][1000 genomes] |
rs61896965 | 0.86[EUR][1000 genomes] |
rs61896966 | 0.86[EUR][1000 genomes] |
rs61897481 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61897558 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs61897559 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs7104912 | 0.81[EUR][1000 genomes] |
rs7113601 | 0.81[EUR][1000 genomes] |
rs7114852 | 0.86[EUR][1000 genomes] |
rs7118321 | 1.00[AFR][1000 genomes] |
rs7128453 | 0.83[EUR][1000 genomes] |
rs7131505 | 0.81[EUR][1000 genomes] |
rs7131616 | 0.81[EUR][1000 genomes] |
rs7925870 | 0.86[EUR][1000 genomes] |
rs7926784 | 0.86[EUR][1000 genomes] |
rs7929811 | 0.86[EUR][1000 genomes] |
rs7931694 | 0.86[EUR][1000 genomes] |
rs7935009 | 0.86[EUR][1000 genomes] |
rs7937610 | 0.86[EUR][1000 genomes] |
rs7942859 | 0.86[EUR][1000 genomes] |
rs7942981 | 0.86[EUR][1000 genomes] |
rs7945499 | 0.86[EUR][1000 genomes] |
rs7949262 | 0.86[EUR][1000 genomes] |
rs7951100 | 1.00[AFR][1000 genomes] |
rs9666864 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs9667335 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs9667688 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs9667699 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv554797 | chr11:55035411-55864161 | Enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 59 gene(s) | inside rSNPs | diseases |
2 | nsv554800 | chr11:55083434-55695985 | ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 42 gene(s) | inside rSNPs | diseases |
3 | nsv1067779 | chr11:55086995-55980406 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 66 gene(s) | inside rSNPs | diseases |
4 | nsv491694 | chr11:55086995-55980406 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 66 gene(s) | inside rSNPs | diseases |
5 | nsv821668 | chr11:55153930-55816828 | Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 46 gene(s) | inside rSNPs | diseases |
6 | nsv1036666 | chr11:55460788-56010187 | ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 44 gene(s) | inside rSNPs | diseases |
7 | nsv1049004 | chr11:55460788-56014767 | Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 45 gene(s) | inside rSNPs | diseases |
8 | esv2830217 | chr11:55460788-56017908 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 45 gene(s) | inside rSNPs | diseases |
9 | nsv1043441 | chr11:55468512-56010187 | Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 44 gene(s) | inside rSNPs | diseases |
10 | nsv1044174 | chr11:55501796-55862172 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 27 gene(s) | inside rSNPs | diseases |
11 | nsv832158 | chr11:55550160-55701309 | ZNF genes & repeats Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
12 | nsv972028 | chr11:55634700-55663452 | ZNF genes & repeats Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS | TF binding regionCpG islandlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:55638000-55640200 | Weak transcription | Brain Inferior Temporal Lobe | brain |