Variant report
Variant | rs17052142 |
---|---|
Chromosome Location | chr16:34809898-34809899 |
allele | C/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] |
---|---|
rs1094595 | 0.83[EUR][1000 genomes] |
rs11861245 | 1.00[CEU][hapmap];0.83[EUR][1000 genomes] |
rs11862087 | 1.00[CEU][hapmap];0.95[YRI][hapmap];0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs11862741 | 0.86[EUR][1000 genomes] |
rs11863543 | 0.86[EUR][1000 genomes] |
rs11864600 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs11865286 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11865574 | 1.00[CEU][hapmap];0.90[YRI][hapmap] |
rs11865764 | 0.90[YRI][hapmap];1.00[EUR][1000 genomes] |
rs11865988 | 1.00[CEU][hapmap] |
rs13331101 | 1.00[EUR][1000 genomes] |
rs1501465 | 0.86[EUR][1000 genomes] |
rs1532679 | 0.86[EUR][1000 genomes] |
rs1583338 | 0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17052144 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17052149 | 1.00[CEU][hapmap] |
rs17052150 | 1.00[CEU][hapmap] |
rs17841547 | 0.86[YRI][hapmap] |
rs17841548 | 1.00[CEU][hapmap];0.95[YRI][hapmap];0.86[EUR][1000 genomes] |
rs17841551 | 0.86[EUR][1000 genomes] |
rs17841552 | 0.86[EUR][1000 genomes] |
rs17841553 | 1.00[CEU][hapmap];0.87[YRI][hapmap];0.86[EUR][1000 genomes] |
rs17841557 | 0.86[EUR][1000 genomes] |
rs17841560 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs17841561 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs17841567 | 1.00[CEU][hapmap] |
rs17841578 | 0.83[EUR][1000 genomes] |
rs237988 | 0.83[EUR][1000 genomes] |
rs237991 | 0.83[EUR][1000 genomes] |
rs28710220 | 0.83[EUR][1000 genomes] |
rs345553 | 0.86[EUR][1000 genomes] |
rs35852265 | 0.83[EUR][1000 genomes] |
rs41466646 | 1.00[EUR][1000 genomes] |
rs55947128 | 0.84[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs55990867 | 0.86[EUR][1000 genomes] |
rs56130601 | 0.86[EUR][1000 genomes] |
rs56150069 | 0.82[AFR][1000 genomes];0.80[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs56789577 | 0.86[EUR][1000 genomes] |
rs57748740 | 0.85[AFR][1000 genomes];0.80[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs58227353 | 0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58334121 | 0.83[EUR][1000 genomes] |
rs58874752 | 1.00[EUR][1000 genomes] |
rs59423657 | 1.00[EUR][1000 genomes] |
rs59902571 | 1.00[EUR][1000 genomes] |
rs59970187 | 0.86[EUR][1000 genomes] |
rs59987957 | 0.80[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs60510786 | 0.88[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs60628599 | 0.86[EUR][1000 genomes] |
rs61287001 | 0.83[EUR][1000 genomes] |
rs61485382 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs61649499 | 0.86[EUR][1000 genomes] |
rs6563877 | 0.82[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs6563878 | 0.86[EUR][1000 genomes] |
rs7185642 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7186375 | 0.86[EUR][1000 genomes] |
rs7186948 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs7192596 | 0.86[EUR][1000 genomes] |
rs7194464 | 0.86[EUR][1000 genomes] |
rs7197316 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs7197656 | 0.86[EUR][1000 genomes] |
rs7198853 | 0.85[AFR][1000 genomes];0.80[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs7198892 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs7202195 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs7204365 | 0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74015953 | 1.00[EUR][1000 genomes] |
rs74015990 | 0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74015992 | 0.86[EUR][1000 genomes] |
rs74015994 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs74015995 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74015996 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs74018403 | 0.86[EUR][1000 genomes] |
rs74018404 | 0.86[EUR][1000 genomes] |
rs74018407 | 0.86[EUR][1000 genomes] |
rs74018408 | 0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74018409 | 0.82[AFR][1000 genomes];0.80[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs74018410 | 0.82[AFR][1000 genomes];0.80[AMR][1000 genomes] |
rs74018412 | 0.80[AMR][1000 genomes] |
rs74018425 | 0.86[EUR][1000 genomes] |
rs74018431 | 0.86[EUR][1000 genomes] |
rs74018433 | 0.86[EUR][1000 genomes] |
rs74018435 | 1.00[EUR][1000 genomes] |
rs74018436 | 0.88[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs74018437 | 0.86[EUR][1000 genomes] |
rs74018438 | 0.86[EUR][1000 genomes] |
rs74018442 | 0.86[EUR][1000 genomes] |
rs74018444 | 0.86[EUR][1000 genomes] |
rs74018445 | 0.85[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs74018456 | 0.86[EUR][1000 genomes] |
rs74018457 | 1.00[EUR][1000 genomes] |
rs74018458 | 1.00[EUR][1000 genomes] |
rs74018459 | 0.86[EUR][1000 genomes] |
rs74018461 | 1.00[EUR][1000 genomes] |
rs74018462 | 1.00[EUR][1000 genomes] |
rs74018463 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs74018464 | 0.82[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs74018465 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs74018468 | 0.85[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs74018469 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs74018470 | 1.00[EUR][1000 genomes] |
rs74018471 | 1.00[EUR][1000 genomes] |
rs74018473 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs7499906 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs7500529 | 1.00[EUR][1000 genomes] |
rs8045492 | 0.86[EUR][1000 genomes] |
rs8045606 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs8048302 | 1.00[CEU][hapmap];0.83[EUR][1000 genomes] |
rs8051145 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs8053475 | 0.86[EUR][1000 genomes] |
rs8054064 | 0.86[EUR][1000 genomes] |
rs8054608 | 0.86[EUR][1000 genomes] |
rs8057388 | 0.86[EUR][1000 genomes] |
rs8058675 | 0.86[EUR][1000 genomes] |
rs8059170 | 0.86[EUR][1000 genomes] |
rs8059333 | 0.88[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs8059400 | 0.86[EUR][1000 genomes] |
rs9783770 | 1.00[CEU][hapmap] |
rs979576 | 1.00[CEU][hapmap];0.86[EUR][1000 genomes] |
rs9921179 | 0.86[EUR][1000 genomes] |
rs9921911 | 0.83[EUR][1000 genomes] |
rs9926843 | 0.83[EUR][1000 genomes] |
rs9932621 | 1.00[CEU][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1067686 | chr16:34202088-35147508 | ZNF genes & repeats Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 83 gene(s) | inside rSNPs | diseases |
2 | nsv532260 | chr16:34202088-35147508 | Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 83 gene(s) | inside rSNPs | diseases |
3 | nsv521817 | chr16:34221454-35168832 | Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 81 gene(s) | inside rSNPs | diseases |
4 | nsv521994 | chr16:34221454-35168832 | Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 81 gene(s) | inside rSNPs | diseases |
5 | esv2757636 | chr16:34436185-35042935 | ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 60 gene(s) | inside rSNPs | diseases |
6 | esv34629 | chr16:34449700-35139485 | ZNF genes & repeats Enhancers Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 60 gene(s) | inside rSNPs | diseases |
7 | nsv431464 | chr16:34467499-35122095 | Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 58 gene(s) | inside rSNPs | diseases |
8 | esv34862 | chr16:34467540-35122095 | Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 58 gene(s) | inside rSNPs | diseases |
9 | nsv431488 | chr16:34467540-35139485 | Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 59 gene(s) | inside rSNPs | diseases |
10 | nsv1056617 | chr16:34543711-35283214 | ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 53 gene(s) | inside rSNPs | diseases |
11 | nsv572385 | chr16:34583626-35285582 | ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 51 gene(s) | inside rSNPs | diseases |
12 | nsv833214 | chr16:34657900-34856068 | Flanking Active TSS ZNF genes & repeats Active TSS Enhancers Bivalent/Poised TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
13 | nsv918222 | chr16:34739999-35076660 | Enhancers ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 32 gene(s) | inside rSNPs | diseases |
14 | nsv977088 | chr16:34789235-34989803 | Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 20 gene(s) | inside rSNPs | diseases |
15 | nsv457486 | chr16:34805859-35168832 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 26 gene(s) | inside rSNPs | diseases |
16 | nsv572387 | chr16:34805859-35168832 | Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 26 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr16:34803000-34814000 | ZNF genes & repeats | ES-UCSF4 Cell Line | embryonic stem cell |
2 | chr16:34807600-34810200 | ZNF genes & repeats | iPS DF 19.11 Cell Line | embryonic stem cell |
3 | chr16:34807800-34811600 | ZNF genes & repeats | Fetal Brain Female | brain |
4 | chr16:34808400-34810600 | ZNF genes & repeats | HUES64 Cell Line | embryonic stem cell |