Variant report
Variant | rs1630758 |
---|---|
Chromosome Location | chr6:45161312-45161313 |
allele | A/G |
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 | chr6:45160972..45165246-chr6:45178939..45182549,3 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1159132 | 0.86[EUR][1000 genomes] |
rs1284956 | 0.83[EUR][1000 genomes] |
rs1284957 | 0.97[EUR][1000 genomes] |
rs1284958 | 0.92[EUR][1000 genomes] |
rs1284959 | 0.88[EUR][1000 genomes] |
rs1284963 | 1.00[EUR][1000 genomes] |
rs1284970 | 0.88[EUR][1000 genomes] |
rs1284971 | 1.00[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1284976 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1284977 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1284978 | 0.86[EUR][1000 genomes] |
rs1284981 | 0.88[EUR][1000 genomes] |
rs1284984 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1284985 | 0.88[EUR][1000 genomes] |
rs1284991 | 0.88[EUR][1000 genomes] |
rs1284994 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1284996 | 0.88[EUR][1000 genomes] |
rs1284997 | 1.00[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1284998 | 1.00[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs1285001 | 0.88[EUR][1000 genomes] |
rs1285012 | 0.88[EUR][1000 genomes] |
rs1285015 | 0.88[EUR][1000 genomes] |
rs1285016 | 0.92[EUR][1000 genomes] |
rs1285017 | 0.88[EUR][1000 genomes] |
rs1329708 | 1.00[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs1329712 | 1.00[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1360198 | 0.86[EUR][1000 genomes] |
rs1411150 | 0.88[EUR][1000 genomes] |
rs1475533 | 0.86[EUR][1000 genomes] |
rs1475534 | 0.86[EUR][1000 genomes] |
rs1536906 | 1.00[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs1548285 | 0.86[EUR][1000 genomes] |
rs1576380 | 1.00[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs1576381 | 1.00[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs1625102 | 0.88[EUR][1000 genomes] |
rs1629619 | 0.88[EUR][1000 genomes] |
rs1632504 | 0.88[EUR][1000 genomes] |
rs1748241 | 1.00[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1748246 | 0.88[EUR][1000 genomes] |
rs1797155 | 0.88[EUR][1000 genomes] |
rs1797157 | 0.88[EUR][1000 genomes] |
rs1797160 | 0.88[EUR][1000 genomes] |
rs1797162 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2183295 | 0.86[EUR][1000 genomes] |
rs2396378 | 1.00[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs2763135 | 0.92[EUR][1000 genomes] |
rs4296887 | 0.83[EUR][1000 genomes] |
rs4323299 | 0.88[EUR][1000 genomes] |
rs4437465 | 0.88[EUR][1000 genomes] |
rs4452642 | 0.88[EUR][1000 genomes] |
rs4469289 | 0.92[EUR][1000 genomes] |
rs4520015 | 0.89[EUR][1000 genomes] |
rs4711811 | 0.88[EUR][1000 genomes] |
rs4711812 | 0.88[EUR][1000 genomes] |
rs4714831 | 1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs4714835 | 1.00[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs4714849 | 0.87[EUR][1000 genomes] |
rs56000304 | 0.92[EUR][1000 genomes] |
rs56051040 | 0.92[EUR][1000 genomes] |
rs56142650 | 0.92[EUR][1000 genomes] |
rs56300352 | 0.92[EUR][1000 genomes] |
rs6458416 | 0.86[EUR][1000 genomes] |
rs6903524 | 0.81[EUR][1000 genomes] |
rs6908280 | 1.00[EUR][1000 genomes] |
rs6912845 | 0.88[EUR][1000 genomes] |
rs6932726 | 0.86[EUR][1000 genomes] |
rs6933742 | 1.00[EUR][1000 genomes] |
rs72857063 | 0.92[EUR][1000 genomes] |
rs72858503 | 0.92[EUR][1000 genomes] |
rs72858507 | 0.92[EUR][1000 genomes] |
rs72869128 | 1.00[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs72869130 | 1.00[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs72869143 | 1.00[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs7739872 | 0.86[EUR][1000 genomes] |
rs7753900 | 0.88[EUR][1000 genomes] |
rs7756721 | 1.00[EUR][1000 genomes] |
rs7763079 | 1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs7765383 | 0.83[EUR][1000 genomes] |
rs7775597 | 1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs9296454 | 1.00[EUR][1000 genomes] |
rs9349320 | 0.83[EUR][1000 genomes] |
rs9357465 | 0.88[EUR][1000 genomes] |
rs9357468 | 0.88[EUR][1000 genomes] |
rs9369527 | 0.86[EUR][1000 genomes] |
rs9369554 | 0.83[EUR][1000 genomes] |
rs9369557 | 0.86[EUR][1000 genomes] |
rs9381356 | 1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs9381363 | 0.88[EUR][1000 genomes] |
rs9395061 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs9472429 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9472430 | 1.00[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs9472459 | 0.94[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1028393 | chr6:44875558-45822335 | Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
2 | nsv538211 | chr6:44875558-45822335 | ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
3 | nsv1024370 | chr6:44878053-45251451 | Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
4 | nsv885864 | chr6:44890760-45198796 | Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
5 | nsv492309 | chr6:45020402-45233484 | Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
6 | nsv1032906 | chr6:45069368-45212863 | ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:45153800-45163000 | Weak transcription | Psoas Muscle | Psoas |
2 | chr6:45155400-45163000 | Weak transcription | Primary T killer naive cells fromperipheralblood | blood |
3 | chr6:45156400-45162000 | Weak transcription | Dnd41 | blood |
4 | chr6:45159600-45163800 | Weak transcription | Liver | Liver |
5 | chr6:45160000-45167000 | Weak transcription | Fetal Intestine Small | intestine |
6 | chr6:45160200-45166000 | Weak transcription | HepG2 | liver |
7 | chr6:45160600-45167000 | Weak transcription | Fetal Intestine Large | intestine |