Variant report
| Variant | rs58893558 |
|---|---|
| Chromosome Location | chr10:50335442-50335443 |
| allele | A/C |
| 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 | chr10:50331517..50334584-chr10:50334823..50337870,3 | K562 | blood: |
| No data |
| No data |
| No data |
| No data |
| rs_ID | r2[population] |
|---|---|
| rs11100988 | 0.81[ASN][1000 genomes] |
| rs11100989 | 0.97[ASN][1000 genomes] |
| rs11100990 | 0.97[ASN][1000 genomes] |
| rs12240534 | 0.94[ASN][1000 genomes] |
| rs12244666 | 0.81[EUR][1000 genomes] |
| rs12244748 | 0.81[EUR][1000 genomes] |
| rs12253426 | 0.81[EUR][1000 genomes] |
| rs12255055 | 0.94[ASN][1000 genomes] |
| rs12255090 | 0.81[EUR][1000 genomes] |
| rs12256777 | 0.82[EUR][1000 genomes] |
| rs12257242 | 0.86[EUR][1000 genomes] |
| rs12261297 | 0.83[EUR][1000 genomes] |
| rs12267388 | 0.97[ASN][1000 genomes] |
| rs12765281 | 0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes] |
| rs12769361 | 0.86[EUR][1000 genomes] |
| rs12776460 | 0.86[EUR][1000 genomes] |
| rs12776553 | 0.95[ASN][1000 genomes] |
| rs17011744 | 0.82[EUR][1000 genomes] |
| rs17011746 | 0.82[EUR][1000 genomes] |
| rs17011757 | 0.83[EUR][1000 genomes] |
| rs17700872 | 0.86[EUR][1000 genomes] |
| rs17701186 | 0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes] |
| rs17773851 | 0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes] |
| rs17782733 | 0.94[ASN][1000 genomes] |
| rs1986725 | 0.90[ASN][1000 genomes] |
| rs2003044 | 0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes] |
| rs2490838 | 0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes] |
| rs2725179 | 0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes] |
| rs2725181 | 0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes] |
| rs2725184 | 0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes] |
| rs2725185 | 0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes] |
| rs2725190 | 0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes] |
| rs2804931 | 0.81[ASN][1000 genomes] |
| rs2804934 | 0.83[ASN][1000 genomes] |
| rs2804937 | 0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |
| rs2804939 | 0.90[ASN][1000 genomes] |
| rs2804940 | 0.90[ASN][1000 genomes] |
| rs2804941 | 0.91[ASN][1000 genomes] |
| rs34056748 | 1.00[ASN][1000 genomes] |
| rs34062275 | 0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes] |
| rs34110351 | 0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes] |
| rs34289781 | 0.85[EUR][1000 genomes] |
| rs34364659 | 0.86[EUR][1000 genomes] |
| rs34436721 | 0.91[ASN][1000 genomes] |
| rs34467986 | 0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes] |
| rs34574986 | 0.86[EUR][1000 genomes] |
| rs34589684 | 0.92[ASN][1000 genomes] |
| rs34640094 | 0.86[EUR][1000 genomes] |
| rs34786393 | 1.00[ASN][1000 genomes] |
| rs34878380 | 0.86[EUR][1000 genomes] |
| rs35007047 | 0.97[ASN][1000 genomes] |
| rs35285557 | 0.95[ASN][1000 genomes] |
| rs35341824 | 0.82[EUR][1000 genomes] |
| rs35462783 | 0.81[EUR][1000 genomes] |
| rs35666409 | 0.95[ASN][1000 genomes] |
| rs35922675 | 0.86[EUR][1000 genomes] |
| rs4073138 | 0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes] |
| rs4073139 | 0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes] |
| rs4073711 | 0.93[ASN][1000 genomes] |
| rs4240500 | 0.83[ASN][1000 genomes] |
| rs4350286 | 0.99[ASN][1000 genomes] |
| rs4364979 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes] |
| rs4400713 | 0.82[EUR][1000 genomes] |
| rs4402204 | 0.81[EUR][1000 genomes] |
| rs4412679 | 0.81[ASN][1000 genomes] |
| rs4417190 | 0.83[ASN][1000 genomes] |
| rs4445564 | 0.84[EUR][1000 genomes] |
| rs4495812 | 0.91[ASN][1000 genomes] |
| rs4497320 | 0.97[ASN][1000 genomes] |
| rs4508127 | 0.83[EUR][1000 genomes] |
| rs4532948 | 0.81[ASN][1000 genomes] |
| rs4600129 | 0.83[EUR][1000 genomes] |
| rs4620641 | 0.83[ASN][1000 genomes] |
| rs4644582 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
| rs4838447 | 0.81[ASN][1000 genomes] |
| rs55947405 | 0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes] |
| rs56291725 | 0.86[EUR][1000 genomes] |
| rs58154726 | 0.85[EUR][1000 genomes] |
| rs67269950 | 0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes] |
| rs68065270 | 0.85[EUR][1000 genomes] |
| rs7070387 | 0.80[EUR][1000 genomes] |
| rs7073208 | 0.81[EUR][1000 genomes] |
| rs7081243 | 0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes] |
| rs7085823 | 0.82[EUR][1000 genomes] |
| rs7088718 | 0.81[EUR][1000 genomes] |
| rs7100655 | 0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes] |
| rs72785015 | 0.86[EUR][1000 genomes] |
| rs7896344 | 0.80[EUR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | esv2761593 | chr10:50276812-50336129 | Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
| 2 | nsv895375 | chr10:50306386-51028871 | Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 33 gene(s) | inside rSNPs | diseases |
| 3 | esv1824894 | chr10:50309905-50340304 | Genic enhancers Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
| 4 | nsv534410 | chr10:50317458-50826916 | Weak transcription Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 30 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr10:50324000-50343600 | Weak transcription | Right Atrium | heart |
| 2 | chr10:50325000-50338600 | Weak transcription | Fetal Muscle Trunk | muscle |
| 3 | chr10:50325000-50339400 | Weak transcription | Ovary | ovary |
| 4 | chr10:50333000-50336000 | Weak transcription | Fetal Muscle Leg | muscle |
| 5 | chr10:50333000-50336200 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |





