Variant report
Variant | rs6933002 |
---|---|
Chromosome Location | chr6:68505458-68505459 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10223522 | 0.91[ASN][1000 genomes] |
rs10223623 | 0.91[ASN][1000 genomes] |
rs11750959 | 0.80[EUR][1000 genomes] |
rs12214983 | 0.92[YRI][hapmap];0.87[AFR][1000 genomes] |
rs12524662 | 0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs13200085 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13215798 | 0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1606681 | 0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1606684 | 0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs16880598 | 0.89[ASN][1000 genomes] |
rs1913477 | 0.80[EUR][1000 genomes] |
rs1913478 | 0.80[EUR][1000 genomes] |
rs2063737 | 0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs34124069 | 0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34125381 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34528887 | 0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34909337 | 0.89[ASN][1000 genomes] |
rs35459134 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4259236 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs56285162 | 0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs57219296 | 0.91[ASN][1000 genomes] |
rs6455248 | 1.00[ASN][1000 genomes] |
rs6455250 | 0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6901396 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs6901505 | 0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs6906512 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6910355 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6913405 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6913540 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6914109 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6920063 | 0.91[ASN][1000 genomes] |
rs6925379 | 0.91[ASN][1000 genomes] |
rs6925414 | 0.91[ASN][1000 genomes] |
rs6927559 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6933191 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6933666 | 0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6940575 | 0.91[ASN][1000 genomes] |
rs6941472 | 0.91[ASN][1000 genomes] |
rs73444607 | 0.91[ASN][1000 genomes] |
rs73444610 | 0.91[ASN][1000 genomes] |
rs73444633 | 0.89[ASN][1000 genomes] |
rs73446734 | 1.00[ASN][1000 genomes] |
rs73462635 | 0.94[ASN][1000 genomes] |
rs73462660 | 1.00[ASN][1000 genomes] |
rs7741697 | 1.00[ASN][1000 genomes] |
rs7750694 | 0.91[ASN][1000 genomes] |
rs7755118 | 0.91[ASN][1000 genomes] |
rs7756292 | 0.91[ASN][1000 genomes] |
rs7760466 | 0.91[ASN][1000 genomes] |
rs7763531 | 1.00[ASN][1000 genomes] |
rs7765314 | 0.91[ASN][1000 genomes] |
rs7769657 | 0.91[ASN][1000 genomes] |
rs9294775 | 1.00[ASN][1000 genomes] |
rs9294776 | 1.00[ASN][1000 genomes] |
rs9445916 | 1.00[ASN][1000 genomes] |
rs9445917 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9454284 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9454286 | 0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9454287 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9454301 | 0.89[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1027923 | chr6:67830533-68828337 | Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
2 | nsv1016471 | chr6:67854363-68708368 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
3 | nsv538292 | chr6:67854363-68708368 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
4 | nsv603589 | chr6:67975166-68865718 | ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
5 | esv2759439 | chr6:68156441-68526511 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
6 | esv2757176 | chr6:68269956-68526511 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
7 | nsv886115 | chr6:68341629-68644319 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
8 | nsv886116 | chr6:68356291-68607744 | Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
9 | nsv886117 | chr6:68380125-68526511 | Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
10 | nsv886120 | chr6:68384242-68509062 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
11 | nsv886121 | chr6:68384242-68526511 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
12 | nsv886122 | chr6:68397567-68526511 | Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
13 | nsv603593 | chr6:68410039-68509062 | ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
14 | nsv603594 | chr6:68417147-68509062 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
15 | esv34754 | chr6:68417692-68532979 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
16 | nsv886124 | chr6:68423329-68505842 | ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
17 | nsv886125 | chr6:68423329-68526511 | ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
18 | nsv886126 | chr6:68449430-68526511 | Weak transcription Enhancers ZNF genes & repeats Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
19 | nsv1032151 | chr6:68455238-68509030 | Enhancers Active TSS Weak transcription ZNF genes & repeats | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
20 | nsv463144 | chr6:68470086-68563328 | Weak transcription Enhancers ZNF genes & repeats Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
21 | nsv603596 | chr6:68470086-68563328 | Enhancers ZNF genes & repeats Active TSS Weak transcription | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
22 | nsv1026831 | chr6:68486914-68509030 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
23 | nsv966631 | chr6:68495364-68505735 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
24 | nsv603597 | chr6:68499138-68542695 | Enhancers ZNF genes & repeats Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:68505000-68506200 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
2 | chr6:68505200-68506000 | Enhancers | H9 Cell Line | embryonic stem cell |
3 | chr6:68505200-68506000 | Enhancers | HUES48 Cell Line | embryonic stem cell |
4 | chr6:68505200-68506000 | Enhancers | HUES6 Cell Line | embryonic stem cell |
5 | chr6:68505200-68506000 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
6 | chr6:68505400-68506400 | Enhancers | K562 | blood |