Variant report
Variant | rs7725419 |
---|---|
Chromosome Location | chr5:94769159-94769160 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:3 , 50 per page) page:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000225165 | Chromatin interaction |
ENSG00000153347 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10036119 | 0.88[ASN][1000 genomes] |
rs10036691 | 0.85[ASN][1000 genomes] |
rs10040367 | 0.88[ASN][1000 genomes] |
rs10045714 | 0.88[ASN][1000 genomes] |
rs10055673 | 0.92[ASN][1000 genomes] |
rs10056208 | 0.88[ASN][1000 genomes] |
rs10056278 | 0.88[ASN][1000 genomes] |
rs10057391 | 0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs10057420 | 0.88[ASN][1000 genomes] |
rs10063417 | 0.88[ASN][1000 genomes] |
rs10070711 | 0.86[ASN][1000 genomes] |
rs10075022 | 0.86[ASN][1000 genomes] |
rs10077070 | 0.88[ASN][1000 genomes] |
rs10223061 | 0.86[ASN][1000 genomes] |
rs10223134 | 0.88[ASN][1000 genomes] |
rs10223147 | 0.88[ASN][1000 genomes] |
rs10476648 | 0.88[ASN][1000 genomes] |
rs10476649 | 0.88[ASN][1000 genomes] |
rs10476652 | 0.85[ASN][1000 genomes] |
rs10476653 | 0.85[ASN][1000 genomes] |
rs10476654 | 0.85[ASN][1000 genomes] |
rs10491246 | 0.81[ASN][1000 genomes] |
rs10515228 | 0.89[ASN][1000 genomes] |
rs1062073 | 0.88[ASN][1000 genomes] |
rs1062075 | 0.84[ASN][1000 genomes] |
rs1062077 | 0.84[ASN][1000 genomes] |
rs1062083 | 0.84[ASN][1000 genomes] |
rs10866765 | 0.86[ASN][1000 genomes] |
rs11135426 | 0.88[ASN][1000 genomes] |
rs11135429 | 0.86[ASN][1000 genomes] |
rs1139111 | 0.88[ASN][1000 genomes] |
rs1139114 | 0.88[ASN][1000 genomes] |
rs11948407 | 0.88[ASN][1000 genomes] |
rs11948489 | 0.86[ASN][1000 genomes] |
rs11949044 | 0.88[ASN][1000 genomes] |
rs11950190 | 0.88[ASN][1000 genomes] |
rs11953160 | 0.85[ASN][1000 genomes] |
rs11953633 | 0.88[ASN][1000 genomes] |
rs11958720 | 0.89[ASN][1000 genomes] |
rs11959401 | 0.89[ASN][1000 genomes] |
rs12054689 | 0.88[ASN][1000 genomes] |
rs12054916 | 0.88[ASN][1000 genomes] |
rs12055264 | 0.86[ASN][1000 genomes] |
rs12189111 | 0.86[ASN][1000 genomes] |
rs13355280 | 0.92[ASN][1000 genomes] |
rs17084769 | 0.88[ASN][1000 genomes] |
rs17084779 | 0.88[ASN][1000 genomes] |
rs17084816 | 0.88[ASN][1000 genomes] |
rs17084817 | 0.88[ASN][1000 genomes] |
rs17084839 | 0.88[ASN][1000 genomes] |
rs17084852 | 0.88[ASN][1000 genomes] |
rs17084867 | 0.89[ASN][1000 genomes] |
rs17084873 | 0.86[ASN][1000 genomes] |
rs17084904 | 0.89[ASN][1000 genomes] |
rs17084909 | 0.87[ASN][1000 genomes] |
rs17084927 | 0.84[ASN][1000 genomes] |
rs2042871 | 0.88[ASN][1000 genomes] |
rs2278224 | 0.92[ASN][1000 genomes] |
rs2303649 | 0.89[ASN][1000 genomes] |
rs2303650 | 0.89[ASN][1000 genomes] |
rs28376538 | 0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs28491117 | 0.95[ASN][1000 genomes] |
rs3776875 | 0.88[ASN][1000 genomes] |
rs3776876 | 0.88[ASN][1000 genomes] |
rs3822616 | 0.88[ASN][1000 genomes] |
rs3822617 | 0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs3822618 | 0.84[ASN][1000 genomes] |
rs3849752 | 0.88[ASN][1000 genomes] |
rs3849753 | 0.84[ASN][1000 genomes] |
rs3849754 | 0.88[ASN][1000 genomes] |
rs3849755 | 0.88[ASN][1000 genomes] |
rs3931769 | 0.88[ASN][1000 genomes] |
rs55679859 | 0.88[ASN][1000 genomes] |
rs58373522 | 0.86[ASN][1000 genomes] |
rs58405178 | 0.86[ASN][1000 genomes] |
rs60954465 | 0.89[ASN][1000 genomes] |
rs6556874 | 0.88[ASN][1000 genomes] |
rs6556876 | 0.86[ASN][1000 genomes] |
rs6866194 | 0.86[ASN][1000 genomes] |
rs6878974 | 0.89[ASN][1000 genomes] |
rs6880676 | 0.83[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs6881618 | 0.85[ASN][1000 genomes] |
rs6891486 | 0.85[ASN][1000 genomes] |
rs6897586 | 0.85[ASN][1000 genomes] |
rs73141954 | 0.95[ASN][1000 genomes] |
rs73143969 | 0.88[ASN][1000 genomes] |
rs73143972 | 0.82[ASN][1000 genomes] |
rs73143974 | 0.88[ASN][1000 genomes] |
rs73145973 | 0.84[ASN][1000 genomes] |
rs73145974 | 0.88[ASN][1000 genomes] |
rs73145991 | 0.88[ASN][1000 genomes] |
rs73777201 | 0.83[ASN][1000 genomes] |
rs73777219 | 0.86[ASN][1000 genomes] |
rs73777221 | 0.86[ASN][1000 genomes] |
rs73778853 | 0.88[ASN][1000 genomes] |
rs7703285 | 0.85[ASN][1000 genomes] |
rs7703948 | 0.88[ASN][1000 genomes] |
rs7705862 | 0.88[ASN][1000 genomes] |
rs7706837 | 0.88[ASN][1000 genomes] |
rs7707851 | 0.88[ASN][1000 genomes] |
rs7707854 | 0.88[ASN][1000 genomes] |
rs7709709 | 0.89[ASN][1000 genomes] |
rs7709828 | 0.88[ASN][1000 genomes] |
rs7710228 | 0.95[ASN][1000 genomes] |
rs7715350 | 0.89[ASN][1000 genomes] |
rs7722225 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7722969 | 0.88[ASN][1000 genomes] |
rs7723951 | 0.88[ASN][1000 genomes] |
rs7724147 | 0.88[ASN][1000 genomes] |
rs7724683 | 0.88[ASN][1000 genomes] |
rs7724730 | 0.88[ASN][1000 genomes] |
rs7725190 | 0.88[ASN][1000 genomes] |
rs7725219 | 0.88[ASN][1000 genomes] |
rs7727453 | 0.88[ASN][1000 genomes] |
rs7727455 | 0.84[ASN][1000 genomes] |
rs7727608 | 0.86[ASN][1000 genomes] |
rs7733476 | 0.88[ASN][1000 genomes] |
rs7737266 | 0.89[ASN][1000 genomes] |
rs890739 | 0.86[ASN][1000 genomes] |
rs9285017 | 0.88[ASN][1000 genomes] |
rs9314142 | 0.88[ASN][1000 genomes] |
rs9314143 | 0.88[ASN][1000 genomes] |
rs9314144 | 0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs9314145 | 0.88[ASN][1000 genomes] |
rs9314146 | 0.88[ASN][1000 genomes] |
rs9314147 | 0.88[ASN][1000 genomes] |
rs9885158 | 0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs9885192 | 0.88[ASN][1000 genomes] |
rs9885291 | 0.84[ASN][1000 genomes] |
rs9885310 | 0.88[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv882388 | chr5:94764006-94925849 | Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:94768600-94776000 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |