Variant report
Variant | rs9363974 |
---|---|
Chromosome Location | chr6:69594614-69594615 |
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] |
---|---|
rs1120509 | 0.87[ASN][1000 genomes] |
rs12055424 | 0.85[ASN][1000 genomes] |
rs12174093 | 0.92[ASN][1000 genomes] |
rs12175526 | 0.84[EUR][1000 genomes] |
rs1403926 | 0.92[ASN][1000 genomes] |
rs1523936 | 0.92[ASN][1000 genomes] |
rs1523938 | 0.85[ASN][1000 genomes] |
rs2224011 | 0.91[ASN][1000 genomes] |
rs2224014 | 0.87[ASN][1000 genomes] |
rs2342760 | 0.87[ASN][1000 genomes] |
rs28594921 | 0.87[ASN][1000 genomes] |
rs4706061 | 0.92[ASN][1000 genomes] |
rs4706710 | 0.87[ASN][1000 genomes] |
rs4706712 | 0.92[ASN][1000 genomes] |
rs472367 | 0.85[ASN][1000 genomes] |
rs478789 | 0.92[ASN][1000 genomes] |
rs480816 | 0.87[ASN][1000 genomes] |
rs482005 | 0.88[ASN][1000 genomes] |
rs482872 | 0.87[ASN][1000 genomes] |
rs483875 | 0.88[ASN][1000 genomes] |
rs483942 | 0.88[ASN][1000 genomes] |
rs484684 | 0.87[ASN][1000 genomes] |
rs484750 | 0.87[ASN][1000 genomes] |
rs485721 | 0.84[ASN][1000 genomes] |
rs486413 | 0.88[ASN][1000 genomes] |
rs487408 | 0.88[ASN][1000 genomes] |
rs487492 | 0.88[ASN][1000 genomes] |
rs489218 | 0.87[ASN][1000 genomes] |
rs491833 | 0.92[ASN][1000 genomes] |
rs491928 | 0.84[ASN][1000 genomes] |
rs492229 | 0.88[ASN][1000 genomes] |
rs492823 | 0.85[ASN][1000 genomes] |
rs492831 | 0.87[ASN][1000 genomes] |
rs492954 | 0.83[ASN][1000 genomes] |
rs493682 | 0.85[ASN][1000 genomes] |
rs493768 | 0.88[ASN][1000 genomes] |
rs496481 | 0.87[ASN][1000 genomes] |
rs497240 | 0.87[ASN][1000 genomes] |
rs497728 | 0.91[ASN][1000 genomes] |
rs499251 | 0.88[ASN][1000 genomes] |
rs500125 | 0.84[ASN][1000 genomes] |
rs501140 | 0.85[ASN][1000 genomes] |
rs501856 | 0.90[ASN][1000 genomes] |
rs504160 | 0.92[ASN][1000 genomes] |
rs505369 | 0.81[ASN][1000 genomes] |
rs505948 | 0.87[ASN][1000 genomes] |
rs506211 | 0.88[ASN][1000 genomes] |
rs507326 | 0.85[ASN][1000 genomes] |
rs508920 | 0.87[ASN][1000 genomes] |
rs509304 | 0.92[ASN][1000 genomes] |
rs509984 | 0.85[ASN][1000 genomes] |
rs510779 | 0.88[ASN][1000 genomes] |
rs512094 | 0.91[ASN][1000 genomes] |
rs512476 | 0.87[ASN][1000 genomes] |
rs513369 | 0.83[ASN][1000 genomes] |
rs514518 | 0.85[ASN][1000 genomes] |
rs514545 | 0.87[ASN][1000 genomes] |
rs522513 | 0.91[ASN][1000 genomes] |
rs523962 | 0.87[ASN][1000 genomes] |
rs525342 | 0.91[ASN][1000 genomes] |
rs527932 | 0.91[ASN][1000 genomes] |
rs528718 | 0.88[ASN][1000 genomes] |
rs529105 | 0.87[ASN][1000 genomes] |
rs530244 | 0.92[ASN][1000 genomes] |
rs533890 | 0.87[ASN][1000 genomes] |
rs536054 | 0.85[ASN][1000 genomes] |
rs536322 | 0.88[ASN][1000 genomes] |
rs538973 | 0.85[ASN][1000 genomes] |
rs539111 | 0.87[ASN][1000 genomes] |
rs540955 | 0.87[ASN][1000 genomes] |
rs540974 | 0.88[ASN][1000 genomes] |
rs541027 | 0.85[ASN][1000 genomes] |
rs542600 | 0.87[ASN][1000 genomes] |
rs542737 | 0.87[ASN][1000 genomes] |
rs544398 | 0.87[ASN][1000 genomes] |
rs547423 | 0.89[ASN][1000 genomes] |
rs550348 | 0.92[ASN][1000 genomes] |
rs550695 | 0.92[ASN][1000 genomes] |
rs551216 | 0.87[ASN][1000 genomes] |
rs551876 | 0.88[ASN][1000 genomes] |
rs552283 | 0.85[ASN][1000 genomes] |
rs553117 | 0.87[ASN][1000 genomes] |
rs553613 | 0.91[ASN][1000 genomes] |
rs555588 | 0.88[ASN][1000 genomes] |
rs555959 | 0.88[ASN][1000 genomes] |
rs558452 | 0.92[ASN][1000 genomes] |
rs562537 | 0.87[ASN][1000 genomes] |
rs563146 | 0.88[ASN][1000 genomes] |
rs563817 | 0.87[ASN][1000 genomes] |
rs564048 | 0.87[ASN][1000 genomes] |
rs566537 | 0.85[ASN][1000 genomes] |
rs568360 | 0.86[ASN][1000 genomes] |
rs570276 | 0.87[ASN][1000 genomes] |
rs570379 | 0.87[ASN][1000 genomes] |
rs571299 | 0.87[ASN][1000 genomes] |
rs573776 | 0.87[ASN][1000 genomes] |
rs577328 | 0.87[ASN][1000 genomes] |
rs577894 | 0.87[ASN][1000 genomes] |
rs579304 | 0.88[ASN][1000 genomes] |
rs579588 | 0.87[ASN][1000 genomes] |
rs579773 | 0.89[ASN][1000 genomes] |
rs580073 | 0.85[ASN][1000 genomes] |
rs580182 | 0.87[ASN][1000 genomes] |
rs580973 | 0.85[ASN][1000 genomes] |
rs6906092 | 0.90[ASN][1000 genomes] |
rs6920573 | 0.91[ASN][1000 genomes] |
rs6927848 | 0.92[ASN][1000 genomes] |
rs6941602 | 0.91[ASN][1000 genomes] |
rs9342736 | 0.91[ASN][1000 genomes] |
rs9346252 | 0.91[ASN][1000 genomes] |
rs9351741 | 0.90[ASN][1000 genomes] |
rs9446070 | 0.84[ASN][1000 genomes] |
rs9454636 | 0.92[ASN][1000 genomes] |
rs9454639 | 0.91[ASN][1000 genomes] |
rs951399 | 0.87[ASN][1000 genomes] |
rs9689807 | 0.85[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv886132 | chr6:69487204-69610281 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
2 | nsv886133 | chr6:69549897-69610281 | Weak transcription Enhancers ZNF genes & repeats Strong transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | nsv886134 | chr6:69571053-69605682 | Weak transcription Enhancers ZNF genes & repeats Strong transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | nsv886135 | chr6:69571053-69606748 | Weak transcription Strong transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | nsv528106 | chr6:69581991-69610281 | Enhancers Weak transcription ZNF genes & repeats Strong transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | nsv470831 | chr6:69581991-69654650 | Weak transcription Enhancers ZNF genes & repeats Strong transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:69590600-69600600 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
2 | chr6:69591600-69602400 | Weak transcription | Brain Inferior Temporal Lobe | brain |
3 | chr6:69592800-69600000 | Weak transcription | Fetal Lung | lung |
4 | chr6:69594000-69600800 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
5 | chr6:69594400-69594800 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |