Variant report
Variant | rs62072168 |
---|---|
Chromosome Location | chr17:15781663-15781664 |
allele | C/G |
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 | chr17:15780272..15782424-chr17:15786424..15788157,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs11651258 | 0.82[ASN][1000 genomes] |
rs11654524 | 0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11655374 | 0.80[ASN][1000 genomes] |
rs11656489 | 0.80[ASN][1000 genomes] |
rs11656518 | 0.80[ASN][1000 genomes] |
rs11658370 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11658454 | 0.85[AFR][1000 genomes];0.91[ASN][1000 genomes] |
rs11658871 | 0.98[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs11870637 | 0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs12051835 | 0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs12603728 | 0.91[ASN][1000 genomes] |
rs12603863 | 0.85[AFR][1000 genomes];0.91[ASN][1000 genomes] |
rs1558409 | 0.85[AFR][1000 genomes] |
rs1613538 | 0.87[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1639394 | 0.84[ASN][1000 genomes] |
rs17776817 | 0.86[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs1797453 | 0.84[ASN][1000 genomes] |
rs1797460 | 0.92[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1797462 | 0.97[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1889021 | 0.97[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs2429742 | 0.84[ASN][1000 genomes] |
rs2535598 | 0.84[ASN][1000 genomes] |
rs2535599 | 0.84[ASN][1000 genomes] |
rs2586557 | 0.90[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs2779187 | 0.83[ASN][1000 genomes] |
rs2787070 | 0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs35743185 | 0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs3744329 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs3744330 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs3859260 | 0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs3925260 | 0.82[ASN][1000 genomes] |
rs4297751 | 0.88[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs4791642 | 0.82[ASN][1000 genomes] |
rs4791653 | 0.85[AFR][1000 genomes];0.86[ASN][1000 genomes] |
rs4792704 | 0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs4792705 | 0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs62071036 | 0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs62071037 | 0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs62071038 | 0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs62072029 | 0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs62072030 | 0.91[ASN][1000 genomes] |
rs62072031 | 0.86[ASN][1000 genomes] |
rs62072032 | 0.85[AFR][1000 genomes];0.91[ASN][1000 genomes] |
rs62072033 | 0.86[ASN][1000 genomes] |
rs62072034 | 0.85[ASN][1000 genomes] |
rs62072052 | 0.80[ASN][1000 genomes] |
rs62072161 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs62072162 | 0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs62072173 | 0.97[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs62072198 | 1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs62072201 | 0.88[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs62072203 | 0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs62072205 | 0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6502475 | 0.94[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs708590 | 0.88[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs708593 | 0.88[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs7214215 | 1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs7218000 | 0.97[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7223657 | 0.81[ASN][1000 genomes] |
rs7503620 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs8076401 | 0.85[ASN][1000 genomes] |
rs8079686 | 0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs8080194 | 0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs859226 | 0.92[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs859228 | 0.91[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs859229 | 0.81[ASN][1000 genomes] |
rs859230 | 0.91[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs859232 | 0.93[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs859233 | 0.83[EUR][1000 genomes] |
rs859234 | 0.94[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs859236 | 0.94[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs859237 | 0.94[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs859238 | 0.94[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs859240 | 0.86[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs859247 | 0.88[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs859248 | 0.88[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs859252 | 0.88[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs859253 | 0.88[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs859255 | 0.87[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs859256 | 0.88[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs859257 | 0.88[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs9893636 | 0.83[ASN][1000 genomes] |
rs9901375 | 0.80[ASN][1000 genomes] |
rs9903682 | 0.80[ASN][1000 genomes] |
rs9907878 | 0.83[ASN][1000 genomes] |
rs9912875 | 0.83[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv916652 | chr17:15093600-15856310 | Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 73 gene(s) | inside rSNPs | diseases |
2 | nsv1059056 | chr17:15294011-15856861 | Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 55 gene(s) | inside rSNPs | diseases |
3 | nsv934185 | chr17:15552960-16551197 | ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 190 gene(s) | inside rSNPs | diseases |
4 | nsv1062951 | chr17:15561070-15890644 | Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 24 gene(s) | inside rSNPs | diseases |
5 | nsv1066023 | chr17:15607267-16053512 | Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 49 gene(s) | inside rSNPs | diseases |
6 | esv3330182 | chr17:15652014-16569534 | Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 177 gene(s) | inside rSNPs | diseases |
7 | esv3446844 | chr17:15654843-16572246 | Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 177 gene(s) | inside rSNPs | diseases |
8 | nsv1061222 | chr17:15672934-15999778 | ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 40 gene(s) | inside rSNPs | diseases |
9 | nsv962264 | chr17:15726145-15784073 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
10 | nsv907706 | chr17:15731923-16056442 | ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 35 gene(s) | inside rSNPs | diseases |
11 | nsv1993 | chr17:15759198-15799029 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
12 | esv1796880 | chr17:15764507-15793669 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
13 | esv1806276 | chr17:15764992-15794687 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr17:15775600-15785400 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
2 | chr17:15780600-15781800 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
3 | chr17:15780800-15782000 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
4 | chr17:15781000-15781800 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
5 | chr17:15781200-15781800 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |