Variant report
Variant | rs298755 |
---|---|
Chromosome Location | chr3:164199354-164199355 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr3:164190398..164192515-chr3:164196627..164199488,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1073608 | 0.83[ASN][1000 genomes] |
rs1084719 | 0.84[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs1084721 | 0.81[ASN][1000 genomes] |
rs13313898 | 0.85[ASN][1000 genomes] |
rs13324218 | 0.85[ASN][1000 genomes] |
rs1347398 | 0.81[ASN][1000 genomes] |
rs1435048 | 0.83[ASN][1000 genomes] |
rs1435049 | 0.83[ASN][1000 genomes] |
rs1435050 | 0.85[ASN][1000 genomes] |
rs1435051 | 0.85[ASN][1000 genomes] |
rs1435052 | 0.85[ASN][1000 genomes] |
rs1513445 | 0.81[ASN][1000 genomes] |
rs1513450 | 0.83[ASN][1000 genomes] |
rs1579577 | 0.83[ASN][1000 genomes] |
rs1579578 | 0.83[ASN][1000 genomes] |
rs1579579 | 0.83[ASN][1000 genomes] |
rs1579580 | 0.83[ASN][1000 genomes] |
rs1600082 | 0.83[ASN][1000 genomes] |
rs1606520 | 0.83[ASN][1000 genomes] |
rs1606521 | 0.83[ASN][1000 genomes] |
rs1611924 | 0.84[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs1615363 | 0.83[ASN][1000 genomes] |
rs1616240 | 0.81[ASN][1000 genomes] |
rs1623011 | 0.81[ASN][1000 genomes] |
rs1626432 | 0.83[ASN][1000 genomes] |
rs1656094 | 0.83[ASN][1000 genomes] |
rs1656096 | 0.83[ASN][1000 genomes] |
rs1656097 | 0.83[ASN][1000 genomes] |
rs1656098 | 0.83[ASN][1000 genomes] |
rs1656099 | 0.83[ASN][1000 genomes] |
rs1656109 | 0.83[ASN][1000 genomes] |
rs1656110 | 0.83[ASN][1000 genomes] |
rs1656111 | 0.83[ASN][1000 genomes] |
rs1656113 | 0.83[ASN][1000 genomes] |
rs1656114 | 0.83[ASN][1000 genomes] |
rs1656115 | 0.83[ASN][1000 genomes] |
rs1656116 | 0.83[ASN][1000 genomes] |
rs1708469 | 0.83[ASN][1000 genomes] |
rs1708470 | 0.83[ASN][1000 genomes] |
rs1708471 | 0.84[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs1708472 | 0.83[ASN][1000 genomes] |
rs1708477 | 0.81[ASN][1000 genomes] |
rs1708482 | 0.83[ASN][1000 genomes] |
rs1708484 | 0.83[ASN][1000 genomes] |
rs1708485 | 0.83[ASN][1000 genomes] |
rs1708486 | 0.83[ASN][1000 genomes] |
rs1708488 | 0.83[ASN][1000 genomes] |
rs1708489 | 0.83[ASN][1000 genomes] |
rs1708490 | 0.83[ASN][1000 genomes] |
rs1708491 | 0.83[ASN][1000 genomes] |
rs1708492 | 0.83[ASN][1000 genomes] |
rs1708493 | 0.83[ASN][1000 genomes] |
rs1708494 | 0.83[ASN][1000 genomes] |
rs1708497 | 0.86[ASN][1000 genomes] |
rs1708498 | 0.83[ASN][1000 genomes] |
rs1708501 | 0.82[ASN][1000 genomes] |
rs1708502 | 0.83[ASN][1000 genomes] |
rs1708503 | 0.83[ASN][1000 genomes] |
rs1708504 | 0.82[ASN][1000 genomes] |
rs1708505 | 0.83[ASN][1000 genomes] |
rs2117533 | 0.81[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs2117535 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs2117536 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs2141852 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs2181 | 0.84[ASN][1000 genomes] |
rs2182 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs2304377 | 0.85[ASN][1000 genomes] |
rs2886570 | 0.84[ASN][1000 genomes] |
rs298741 | 0.83[ASN][1000 genomes] |
rs298742 | 0.83[ASN][1000 genomes] |
rs298743 | 0.83[ASN][1000 genomes] |
rs298744 | 0.83[ASN][1000 genomes] |
rs298745 | 0.83[ASN][1000 genomes] |
rs298746 | 0.86[CHB][hapmap];0.93[CHD][hapmap];0.90[JPT][hapmap];0.83[ASN][1000 genomes] |
rs298747 | 0.86[CHB][hapmap];0.93[CHD][hapmap];0.90[JPT][hapmap];0.83[ASN][1000 genomes] |
rs298756 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs298757 | 0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs298758 | 0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs298759 | 0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs298760 | 0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs367230 | 0.83[ASN][1000 genomes] |
rs378206 | 0.83[ASN][1000 genomes] |
rs3816090 | 0.85[ASN][1000 genomes] |
rs393334 | 0.90[ASN][1000 genomes] |
rs401402 | 0.83[ASN][1000 genomes] |
rs410229 | 0.82[ASN][1000 genomes] |
rs419649 | 0.82[ASN][1000 genomes] |
rs420836 | 0.83[ASN][1000 genomes] |
rs433861 | 0.83[ASN][1000 genomes] |
rs434335 | 0.83[ASN][1000 genomes] |
rs442287 | 0.83[ASN][1000 genomes] |
rs452224 | 0.83[ASN][1000 genomes] |
rs4855177 | 0.83[ASN][1000 genomes] |
rs4855247 | 0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs66465044 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs66949604 | 0.84[ASN][1000 genomes] |
rs67216762 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs67336409 | 0.84[ASN][1000 genomes] |
rs7612403 | 0.82[ASN][1000 genomes] |
rs7618193 | 0.85[ASN][1000 genomes] |
rs7623330 | 0.82[ASN][1000 genomes] |
rs7623591 | 0.82[ASN][1000 genomes] |
rs7625665 | 0.82[ASN][1000 genomes] |
rs7626138 | 0.82[ASN][1000 genomes] |
rs7636354 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs7637477 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs7638296 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs7638502 | 0.84[ASN][1000 genomes] |
rs7639917 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs7639997 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs7640767 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs7648537 | 0.84[ASN][1000 genomes] |
rs7650970 | 0.85[ASN][1000 genomes] |
rs7651057 | 0.85[ASN][1000 genomes] |
rs783583 | 0.81[ASN][1000 genomes] |
rs783584 | 0.81[ASN][1000 genomes] |
rs783585 | 0.81[ASN][1000 genomes] |
rs783586 | 0.84[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs783587 | 0.81[ASN][1000 genomes] |
rs783589 | 0.81[ASN][1000 genomes] |
rs811459 | 0.81[ASN][1000 genomes] |
rs811955 | 0.82[ASN][1000 genomes] |
rs811956 | 0.81[ASN][1000 genomes] |
rs814147 | 0.81[ASN][1000 genomes] |
rs9290232 | 0.83[ASN][1000 genomes] |
rs9835203 | 0.81[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs9835558 | 0.83[ASN][1000 genomes] |
rs9835718 | 0.81[AMR][1000 genomes];0.82[ASN][1000 genomes] |
rs9839722 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs9840047 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs9840091 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs9844292 | 0.84[ASN][1000 genomes] |
rs9844690 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs9855296 | 0.81[ASN][1000 genomes] |
rs9864025 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs9864184 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs9873142 | 0.81[ASN][1000 genomes] |
rs9876091 | 0.81[ASN][1000 genomes] |
rs9882072 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs997207 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs999592 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1009069 | chr3:163787128-164323219 | Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 7 gene(s) | inside rSNPs | diseases |
2 | nsv877840 | chr3:163832988-164200220 | Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv1010490 | chr3:163961100-164399225 | Enhancers Strong transcription ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
4 | nsv497973 | chr3:163970658-164370204 | Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
5 | nsv1014815 | chr3:164007081-164359622 | Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
6 | nsv877893 | chr3:164018044-164202045 | Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
7 | esv1843213 | chr3:164018044-164209573 | Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
8 | nsv1006002 | chr3:164021906-164653572 | Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
9 | nsv998340 | chr3:164047951-164325380 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
10 | nsv999285 | chr3:164133483-164326560 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
11 | nsv536791 | chr3:164133483-164326560 | Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | Chromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
12 | esv2763323 | chr3:164189618-164243301 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:164195200-164202200 | Weak transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |