Variant report
Variant | rs4707236 |
---|---|
Chromosome Location | chr6:86583967-86583968 |
allele | A/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] |
---|---|
rs1018184 | 0.91[EUR][1000 genomes] |
rs10498958 | 0.91[EUR][1000 genomes] |
rs10944157 | 0.80[EUR][1000 genomes] |
rs10944161 | 0.94[EUR][1000 genomes] |
rs10944168 | 0.89[EUR][1000 genomes] |
rs10944169 | 0.89[EUR][1000 genomes] |
rs10944170 | 0.89[EUR][1000 genomes] |
rs11752180 | 0.84[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs11752223 | 0.84[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs11755864 | 0.89[EUR][1000 genomes] |
rs11756615 | 0.90[EUR][1000 genomes] |
rs11756621 | 0.85[EUR][1000 genomes] |
rs11758849 | 0.88[EUR][1000 genomes] |
rs11758864 | 0.94[EUR][1000 genomes] |
rs11759855 | 0.94[EUR][1000 genomes] |
rs12153887 | 0.82[ASN][1000 genomes] |
rs12154056 | 0.94[EUR][1000 genomes] |
rs12190012 | 0.86[EUR][1000 genomes] |
rs12190598 | 0.89[EUR][1000 genomes] |
rs12190735 | 0.83[EUR][1000 genomes] |
rs12192992 | 0.94[EUR][1000 genomes] |
rs12193556 | 0.91[EUR][1000 genomes] |
rs12194747 | 0.91[EUR][1000 genomes] |
rs12195542 | 0.84[EUR][1000 genomes] |
rs12196037 | 0.89[EUR][1000 genomes] |
rs12196377 | 0.81[EUR][1000 genomes] |
rs12197883 | 0.85[EUR][1000 genomes] |
rs12198061 | 0.80[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs12199516 | 0.86[EUR][1000 genomes] |
rs12199784 | 0.86[EUR][1000 genomes] |
rs12199832 | 0.92[EUR][1000 genomes] |
rs12201571 | 0.94[EUR][1000 genomes] |
rs12201741 | 0.97[EUR][1000 genomes] |
rs12201992 | 0.94[EUR][1000 genomes] |
rs12202712 | 0.85[AFR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12205336 | 0.86[EUR][1000 genomes] |
rs12207057 | 0.92[EUR][1000 genomes] |
rs12207305 | 0.86[EUR][1000 genomes] |
rs12209127 | 0.84[EUR][1000 genomes] |
rs12209668 | 0.82[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs12212733 | 0.86[EUR][1000 genomes] |
rs12213149 | 0.91[EUR][1000 genomes] |
rs12215037 | 0.86[EUR][1000 genomes] |
rs12215903 | 0.90[EUR][1000 genomes] |
rs12216203 | 0.90[EUR][1000 genomes] |
rs12216328 | 0.89[EUR][1000 genomes] |
rs12660846 | 0.84[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs12661204 | 0.91[EUR][1000 genomes] |
rs12665464 | 0.84[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs13196930 | 0.92[EUR][1000 genomes] |
rs13199006 | 0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs13200064 | 0.95[EUR][1000 genomes] |
rs13207537 | 0.80[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs13209671 | 0.81[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs13213551 | 0.93[EUR][1000 genomes] |
rs13213603 | 0.81[ASN][1000 genomes] |
rs13216182 | 0.93[EUR][1000 genomes] |
rs13217384 | 0.87[EUR][1000 genomes] |
rs1337843 | 0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1337844 | 0.89[EUR][1000 genomes] |
rs1415753 | 0.86[EUR][1000 genomes] |
rs1447160 | 0.83[ASN][1000 genomes] |
rs1577917 | 0.89[EUR][1000 genomes] |
rs16876540 | 0.94[EUR][1000 genomes] |
rs1813001 | 0.82[ASN][1000 genomes] |
rs1838954 | 0.82[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs1838955 | 0.82[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs1838958 | 0.81[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs1838959 | 0.80[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs1857965 | 0.94[EUR][1000 genomes] |
rs1911553 | 0.94[EUR][1000 genomes] |
rs1962715 | 0.92[EUR][1000 genomes] |
rs1962716 | 0.91[EUR][1000 genomes] |
rs1995688 | 0.94[EUR][1000 genomes] |
rs1999852 | 0.89[EUR][1000 genomes] |
rs2084293 | 0.82[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs2084294 | 0.82[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs2084296 | 0.83[ASN][1000 genomes] |
rs2084297 | 0.83[ASN][1000 genomes] |
rs2100109 | 0.83[ASN][1000 genomes] |
rs2121594 | 0.84[EUR][1000 genomes] |
rs2197648 | 0.83[ASN][1000 genomes] |
rs2218594 | 0.83[ASN][1000 genomes] |
rs2324842 | 0.94[EUR][1000 genomes] |
rs2324843 | 0.94[EUR][1000 genomes] |
rs2660576 | 0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs2816815 | 0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs2875456 | 0.97[EUR][1000 genomes] |
rs28885198 | 0.94[EUR][1000 genomes] |
rs34106666 | 0.90[EUR][1000 genomes] |
rs34258068 | 0.91[EUR][1000 genomes] |
rs34300848 | 0.89[EUR][1000 genomes] |
rs34492764 | 0.93[EUR][1000 genomes] |
rs34581302 | 0.89[EUR][1000 genomes] |
rs34622557 | 0.94[EUR][1000 genomes] |
rs34852683 | 0.89[EUR][1000 genomes] |
rs35038582 | 0.86[EUR][1000 genomes] |
rs35156995 | 0.91[EUR][1000 genomes] |
rs35385043 | 0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs35419329 | 0.89[EUR][1000 genomes] |
rs35738006 | 0.92[EUR][1000 genomes] |
rs35797755 | 0.89[EUR][1000 genomes] |
rs35874630 | 0.83[ASN][1000 genomes] |
rs36035797 | 0.86[ASN][1000 genomes] |
rs36053156 | 0.82[EUR][1000 genomes] |
rs36096931 | 0.89[EUR][1000 genomes] |
rs36138664 | 0.85[EUR][1000 genomes] |
rs4351219 | 0.94[EUR][1000 genomes] |
rs4706252 | 0.86[ASN][1000 genomes] |
rs4706253 | 0.86[ASN][1000 genomes] |
rs4706254 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs4707229 | 0.83[ASN][1000 genomes] |
rs4707239 | 0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6454513 | 0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs6454515 | 0.84[EUR][1000 genomes] |
rs68171315 | 0.89[EUR][1000 genomes] |
rs6914463 | 0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs6923148 | 0.80[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs6933377 | 0.89[EUR][1000 genomes] |
rs6936048 | 0.89[EUR][1000 genomes] |
rs6941138 | 0.82[EUR][1000 genomes] |
rs7739241 | 0.84[AFR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs7747824 | 0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7747897 | 0.92[EUR][1000 genomes] |
rs7755730 | 0.84[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs7760207 | 0.86[EUR][1000 genomes] |
rs7766645 | 0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs7771342 | 0.94[EUR][1000 genomes] |
rs791856 | 0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs884841 | 0.89[EUR][1000 genomes] |
rs884842 | 0.89[EUR][1000 genomes] |
rs9353349 | 0.85[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs955227 | 0.92[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1028293 | chr6:86353958-86778912 | Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 100 gene(s) | inside rSNPs | diseases |
2 | nsv538350 | chr6:86353958-86778912 | Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 100 gene(s) | inside rSNPs | diseases |
3 | nsv886335 | chr6:86445651-86669361 | Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
4 | nsv1022618 | chr6:86465365-87432069 | Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
5 | nsv538352 | chr6:86465365-87432069 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
6 | nsv1033637 | chr6:86482045-86701733 | Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
7 | nsv538353 | chr6:86482045-86701733 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
8 | esv1802672 | chr6:86546123-86662267 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
9 | nsv1018453 | chr6:86555984-86761120 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer | TF binding regionChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
10 | nsv463940 | chr6:86576854-86648436 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
11 | nsv604095 | chr6:86576854-86648436 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
12 | nsv604096 | chr6:86576854-86649705 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
SNP | Gene | Cis/trans | Tissue | Source |
---|---|---|---|---|
rs4707236 | SNHG5 | cis | Heart Left Ventricle | GTEx |
rs4707236 | SNHG5 | cis | Thyroid | GTEx |
rs4707236 | SNHG5 | Cis_1M | lymphoblastoid | RTeQTL |
rs4707236 | SNHG5 | cis | lung | GTEx |
rs4707236 | SNHG5 | cis | Esophagus Mucosa | GTEx |
rs4707236 | SNHG5 | cis | Skin Sun Exposed Lower leg | GTEx |
rs4707236 | SNHG5 | cis | Nerve Tibial | GTEx |
rs4707236 | SNHG5 | cis | Artery Aorta | GTEx |
rs4707236 | SNHG5 | cis | Muscle Skeletal | GTEx |
rs4707236 | SNHG5 | cis | Adipose Subcutaneous | GTEx |
rs4707236 | SNHG5 | cis | multi-tissue | Pritchard |
rs4707236 | SNHG5 | cis | Artery Tibial | GTEx |
rs4707236 | SNHG5 | cis | Whole Blood | GTEx |
rs4707236 | SNHG5 | cis | Esophagus Muscularis | GTEx |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:86579200-86584000 | Weak transcription | Ovary | ovary |