Variant report
Variant | rs16847708 |
---|---|
Chromosome Location | chr3:163849176-163849177 |
allele | A/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] |
---|---|
rs10513605 | 0.80[AMR][1000 genomes] |
rs10804812 | 0.83[AMR][1000 genomes] |
rs10936401 | 0.80[AMR][1000 genomes] |
rs10936402 | 0.80[AMR][1000 genomes] |
rs10936404 | 0.80[AMR][1000 genomes] |
rs10936405 | 0.80[AMR][1000 genomes] |
rs10936406 | 0.80[AMR][1000 genomes] |
rs10936408 | 0.80[AMR][1000 genomes] |
rs10936411 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs11536323 | 0.80[AMR][1000 genomes] |
rs11543537 | 0.80[AMR][1000 genomes] |
rs11706518 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs11706792 | 0.83[AMR][1000 genomes] |
rs11707163 | 0.80[AMR][1000 genomes] |
rs11709197 | 0.80[AMR][1000 genomes] |
rs11710319 | 0.80[AMR][1000 genomes] |
rs11711476 | 0.83[AMR][1000 genomes] |
rs11711705 | 0.80[AMR][1000 genomes] |
rs11712717 | 0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs11714036 | 0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs11715639 | 0.83[AMR][1000 genomes] |
rs11717385 | 0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs11718123 | 0.80[AMR][1000 genomes] |
rs11718667 | 0.83[AMR][1000 genomes] |
rs11719283 | 0.84[AMR][1000 genomes] |
rs11719688 | 0.80[AMR][1000 genomes] |
rs12163632 | 0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs12485817 | 0.80[AMR][1000 genomes] |
rs12486292 | 0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs12486559 | 0.80[AMR][1000 genomes] |
rs12486777 | 0.80[AMR][1000 genomes] |
rs12486898 | 0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs12487512 | 0.80[AMR][1000 genomes] |
rs12487536 | 0.83[AMR][1000 genomes] |
rs12487948 | 0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs12488423 | 0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12488755 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12488823 | 0.81[AMR][1000 genomes] |
rs12489790 | 0.80[AMR][1000 genomes] |
rs12489916 | 0.83[AMR][1000 genomes] |
rs12490006 | 0.80[AMR][1000 genomes] |
rs12490037 | 0.80[AMR][1000 genomes] |
rs12490057 | 0.80[AMR][1000 genomes] |
rs12490826 | 0.80[AMR][1000 genomes] |
rs12490894 | 0.80[AMR][1000 genomes] |
rs12490986 | 0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs12491407 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs12491958 | 0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs12492243 | 0.83[AMR][1000 genomes] |
rs12492246 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs12493169 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12493224 | 0.80[AMR][1000 genomes] |
rs12494841 | 0.83[AMR][1000 genomes] |
rs12494921 | 0.80[AMR][1000 genomes] |
rs12495248 | 0.85[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs12495535 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs12495540 | 0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12495977 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs12496516 | 0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs12496876 | 0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs12497290 | 0.80[AMR][1000 genomes] |
rs12497350 | 0.83[AMR][1000 genomes] |
rs12497621 | 0.80[AMR][1000 genomes] |
rs12629383 | 0.80[AMR][1000 genomes] |
rs12631347 | 0.83[AMR][1000 genomes] |
rs12632056 | 0.80[AMR][1000 genomes] |
rs12632594 | 0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs12634584 | 0.80[AMR][1000 genomes] |
rs12636667 | 0.80[AMR][1000 genomes] |
rs12638057 | 0.83[AMR][1000 genomes] |
rs1321549 | 0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs1349285 | 0.83[AMR][1000 genomes] |
rs1349607 | 0.83[AMR][1000 genomes] |
rs1375832 | 0.83[AMR][1000 genomes] |
rs1375833 | 0.83[AMR][1000 genomes] |
rs1375834 | 0.83[AMR][1000 genomes] |
rs1375835 | 0.83[AMR][1000 genomes] |
rs1375839 | 0.83[AMR][1000 genomes] |
rs1375842 | 0.80[AMR][1000 genomes] |
rs1375843 | 0.80[AMR][1000 genomes] |
rs1375844 | 0.80[AMR][1000 genomes] |
rs1375845 | 0.80[AMR][1000 genomes] |
rs1375846 | 0.80[AMR][1000 genomes] |
rs1407078 | 0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1449921 | 0.80[AMR][1000 genomes] |
rs1449922 | 0.80[AMR][1000 genomes] |
rs1449927 | 1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1449932 | 0.83[AMR][1000 genomes] |
rs1449933 | 0.83[AMR][1000 genomes] |
rs1449934 | 0.83[AMR][1000 genomes] |
rs1449937 | 0.80[AMR][1000 genomes] |
rs1449938 | 0.80[AMR][1000 genomes] |
rs1449940 | 0.80[AMR][1000 genomes] |
rs1452156 | 0.80[AMR][1000 genomes] |
rs1452157 | 0.80[AMR][1000 genomes] |
rs1452160 | 0.80[AMR][1000 genomes] |
rs1452161 | 0.83[AMR][1000 genomes] |
rs1452162 | 0.83[AMR][1000 genomes] |
rs1470669 | 0.80[AMR][1000 genomes] |
rs1470670 | 0.80[AMR][1000 genomes] |
rs1470799 | 0.81[AMR][1000 genomes] |
rs1530755 | 0.80[AMR][1000 genomes] |
rs1584556 | 0.80[AMR][1000 genomes] |
rs1590223 | 0.85[ASN][1000 genomes] |
rs1597402 | 0.80[AMR][1000 genomes] |
rs1597404 | 0.80[AMR][1000 genomes] |
rs16847620 | 0.80[AMR][1000 genomes] |
rs16847629 | 0.83[AMR][1000 genomes] |
rs16847680 | 0.83[AMR][1000 genomes] |
rs16847692 | 0.83[AMR][1000 genomes] |
rs16847698 | 0.83[AMR][1000 genomes] |
rs16847734 | 0.84[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs16847815 | 0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1839412 | 0.83[AMR][1000 genomes] |
rs1839413 | 0.83[AMR][1000 genomes] |
rs1839943 | 0.80[AMR][1000 genomes] |
rs1947343 | 0.80[AMR][1000 genomes] |
rs1992985 | 0.83[AMR][1000 genomes] |
rs1992986 | 0.85[AMR][1000 genomes] |
rs1992987 | 0.83[AMR][1000 genomes] |
rs2122375 | 0.80[AMR][1000 genomes] |
rs2167122 | 0.80[AMR][1000 genomes] |
rs2197949 | 0.80[AMR][1000 genomes] |
rs2198280 | 0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs2218768 | 0.80[AMR][1000 genomes] |
rs2365544 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs2366088 | 0.82[AFR][1000 genomes] |
rs34424956 | 0.81[ASN][1000 genomes] |
rs35351537 | 0.83[AMR][1000 genomes] |
rs35446408 | 0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs35766450 | 0.80[AMR][1000 genomes] |
rs4280642 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs4289352 | 0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs4411886 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4449321 | 0.81[AMR][1000 genomes] |
rs4449322 | 0.83[AMR][1000 genomes] |
rs4521233 | 0.83[AMR][1000 genomes] |
rs4547704 | 0.80[AMR][1000 genomes] |
rs55680832 | 0.81[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs55871417 | 0.80[AMR][1000 genomes] |
rs55912583 | 0.80[AMR][1000 genomes] |
rs55922928 | 0.80[AMR][1000 genomes] |
rs55923107 | 0.83[AMR][1000 genomes] |
rs55943692 | 0.80[AMR][1000 genomes] |
rs56011219 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs56121628 | 0.80[AMR][1000 genomes] |
rs56212321 | 0.80[AMR][1000 genomes] |
rs56322923 | 0.80[AMR][1000 genomes] |
rs56408530 | 0.80[AMR][1000 genomes] |
rs56668299 | 0.80[AMR][1000 genomes] |
rs56739753 | 0.80[AMR][1000 genomes] |
rs59281714 | 0.83[AMR][1000 genomes] |
rs59583312 | 0.80[AMR][1000 genomes] |
rs60419632 | 0.80[AMR][1000 genomes] |
rs60735329 | 0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs722534 | 0.83[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs73170721 | 0.80[AMR][1000 genomes] |
rs73170722 | 0.80[AMR][1000 genomes] |
rs73170724 | 0.80[AMR][1000 genomes] |
rs73170725 | 0.80[AMR][1000 genomes] |
rs73170729 | 0.80[AMR][1000 genomes] |
rs73170748 | 0.80[AMR][1000 genomes] |
rs73170752 | 0.83[AMR][1000 genomes] |
rs73170753 | 0.83[AMR][1000 genomes] |
rs73172621 | 0.83[AMR][1000 genomes] |
rs73172622 | 0.83[AMR][1000 genomes] |
rs73172626 | 0.80[AMR][1000 genomes] |
rs73172632 | 0.80[AMR][1000 genomes] |
rs7429375 | 0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9647384 | 0.83[AMR][1000 genomes] |
rs9647389 | 0.83[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv877820 | chr3:163557163-164167085 | Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
2 | esv2757903 | chr3:163602449-163910060 | Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
3 | esv2759199 | chr3:163602449-163910060 | Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
4 | nsv428097 | chr3:163602449-163910060 | Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
5 | nsv428425 | chr3:163602449-163910060 | Weak transcription Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
6 | nsv877825 | chr3:163620918-164126802 | Flanking Active TSS Active TSS ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
7 | nsv1006270 | chr3:163651905-163849686 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
8 | nsv1002992 | chr3:163670436-163935375 | Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
9 | nsv1012169 | chr3:163673654-163911342 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
10 | nsv997626 | chr3:163747480-163883789 | ZNF genes & repeats Weak transcription Enhancers Strong transcription Genic enhancers | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
11 | nsv997859 | chr3:163751814-163915341 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionChromatin interactive regionmiRNA | 3 gene(s) | inside rSNPs | diseases |
12 | nsv877833 | chr3:163761825-164109377 | Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
13 | 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 |
14 | nsv877834 | chr3:163795964-163981544 | Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionChromatin interactive regionmiRNA | 3 gene(s) | inside rSNPs | diseases |
15 | nsv877835 | chr3:163795964-164018044 | Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS | TF binding regionCpG islandChromatin interactive regionmiRNA | 3 gene(s) | inside rSNPs | diseases |
16 | nsv877836 | chr3:163795964-164109377 | Enhancers Strong transcription Active TSS Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
17 | nsv877837 | chr3:163823186-163930675 | Weak transcription Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionChromatin interactive regionmiRNA | 3 gene(s) | inside rSNPs | diseases |
18 | nsv877838 | chr3:163823186-163981544 | Enhancers Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS | TF binding regionChromatin interactive regionmiRNA | 3 gene(s) | inside rSNPs | diseases |
19 | nsv877839 | chr3:163823186-164126802 | Enhancers Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
20 | nsv1004324 | chr3:163829339-163918909 | ZNF genes & repeats Enhancers Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' | TF binding regionChromatin interactive regionmiRNA | 3 gene(s) | inside rSNPs | diseases |
21 | nsv592435 | chr3:163832166-164138131 | Strong transcription Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
22 | nsv520501 | chr3:163832988-163962485 | Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Active TSS | TF binding regionChromatin interactive regionmiRNA | 3 gene(s) | inside rSNPs | diseases |
23 | 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 |
24 | nsv829783 | chr3:163834874-163983738 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Active TSS | TF binding regionChromatin interactive regionmiRNA | 2 gene(s) | inside rSNPs | diseases |
25 | nsv428746 | chr3:163834875-163983738 | ZNF genes & repeats Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS | TF binding regionChromatin interactive regionmiRNA | 2 gene(s) | inside rSNPs | diseases |
26 | nsv877841 | chr3:163835270-163898428 | Enhancers Strong transcription Weak transcription ZNF genes & repeats | TF binding regionChromatin interactive regionmiRNA | 1 gene(s) | inside rSNPs | diseases |
27 | nsv877842 | chr3:163835270-163910768 | Enhancers Strong transcription Weak transcription ZNF genes & repeats | TF binding regionChromatin interactive regionmiRNA | 2 gene(s) | inside rSNPs | diseases |
28 | nsv877843 | chr3:163835270-164126802 | Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 3 gene(s) | inside rSNPs | diseases |
29 | nsv592436 | chr3:163836487-163895047 | Strong transcription ZNF genes & repeats Enhancers Weak transcription | TF binding regionChromatin interactive regionmiRNA | 1 gene(s) | inside rSNPs | diseases |
30 | nsv877844 | chr3:163836487-163902187 | ZNF genes & repeats Weak transcription Enhancers Strong transcription | TF binding regionChromatin interactive regionmiRNA | 2 gene(s) | inside rSNPs | diseases |
31 | nsv877845 | chr3:163836487-163910768 | Strong transcription Enhancers Weak transcription ZNF genes & repeats | TF binding regionChromatin interactive regionmiRNA | 2 gene(s) | inside rSNPs | diseases |
32 | nsv877846 | chr3:163836487-164018044 | Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Enhancers Weak transcription Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionmiRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:163839200-163852000 | Strong transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
2 | chr3:163848600-163849800 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |