Variant report
Variant | rs10017163 |
---|---|
Chromosome Location | chr4:95770979-95770980 |
allele | A/G/T |
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 | chr4:95763140..95765026-chr4:95770756..95772869,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10003866 | 0.91[ASN][1000 genomes] |
rs10003992 | 0.86[ASN][1000 genomes] |
rs10004286 | 0.81[ASN][1000 genomes] |
rs10004478 | 0.91[ASN][1000 genomes] |
rs10004573 | 0.91[ASN][1000 genomes] |
rs10005096 | 0.92[ASN][1000 genomes] |
rs10005252 | 0.92[ASN][1000 genomes] |
rs10005450 | 0.92[ASN][1000 genomes] |
rs10008126 | 0.81[AMR][1000 genomes] |
rs10010959 | 0.91[ASN][1000 genomes] |
rs10014945 | 0.91[ASN][1000 genomes] |
rs10015222 | 0.91[ASN][1000 genomes] |
rs10017575 | 0.91[ASN][1000 genomes] |
rs10027656 | 0.92[ASN][1000 genomes] |
rs10033559 | 0.92[ASN][1000 genomes] |
rs1003909 | 0.83[ASN][1000 genomes] |
rs10212893 | 0.91[ASN][1000 genomes] |
rs11097441 | 0.81[ASN][1000 genomes] |
rs11097443 | 0.91[ASN][1000 genomes] |
rs11097444 | 0.91[ASN][1000 genomes] |
rs11097445 | 0.91[ASN][1000 genomes] |
rs11934778 | 0.87[ASN][1000 genomes] |
rs11946778 | 0.84[ASN][1000 genomes] |
rs12500280 | 0.86[ASN][1000 genomes] |
rs12500330 | 0.86[ASN][1000 genomes] |
rs12503136 | 0.81[AMR][1000 genomes] |
rs13103529 | 0.91[ASN][1000 genomes] |
rs13117041 | 0.92[ASN][1000 genomes] |
rs13117507 | 0.92[ASN][1000 genomes] |
rs13120681 | 0.81[AMR][1000 genomes] |
rs13127197 | 0.90[ASN][1000 genomes] |
rs13127435 | 0.91[ASN][1000 genomes] |
rs13127833 | 0.91[ASN][1000 genomes] |
rs13127842 | 0.91[ASN][1000 genomes] |
rs13127888 | 0.91[ASN][1000 genomes] |
rs13139046 | 0.84[ASN][1000 genomes] |
rs13149762 | 0.92[ASN][1000 genomes] |
rs13150342 | 0.92[ASN][1000 genomes] |
rs13151193 | 0.91[ASN][1000 genomes] |
rs1319314 | 0.91[ASN][1000 genomes] |
rs1319315 | 0.91[ASN][1000 genomes] |
rs1319316 | 0.91[ASN][1000 genomes] |
rs1544386 | 0.92[ASN][1000 genomes] |
rs1544387 | 0.91[ASN][1000 genomes] |
rs1544388 | 0.89[ASN][1000 genomes] |
rs1544389 | 0.89[ASN][1000 genomes] |
rs1544390 | 0.87[ASN][1000 genomes] |
rs1544391 | 0.88[ASN][1000 genomes] |
rs1544392 | 0.91[ASN][1000 genomes] |
rs1544393 | 0.91[ASN][1000 genomes] |
rs28501174 | 0.81[AMR][1000 genomes] |
rs2865413 | 0.92[ASN][1000 genomes] |
rs4077885 | 0.81[AMR][1000 genomes] |
rs4254781 | 0.91[ASN][1000 genomes] |
rs4256228 | 0.91[ASN][1000 genomes] |
rs4361394 | 0.89[ASN][1000 genomes] |
rs4364269 | 0.91[ASN][1000 genomes] |
rs4429734 | 0.91[ASN][1000 genomes] |
rs4437261 | 0.91[ASN][1000 genomes] |
rs4533780 | 0.82[ASN][1000 genomes] |
rs4538488 | 0.91[ASN][1000 genomes] |
rs6532511 | 0.81[ASN][1000 genomes] |
rs6532512 | 0.91[ASN][1000 genomes] |
rs6812504 | 0.91[ASN][1000 genomes] |
rs6816019 | 0.87[ASN][1000 genomes] |
rs6816482 | 0.87[ASN][1000 genomes] |
rs6817080 | 0.87[ASN][1000 genomes] |
rs6817662 | 0.91[ASN][1000 genomes] |
rs6828291 | 0.92[ASN][1000 genomes] |
rs6828354 | 0.92[ASN][1000 genomes] |
rs6828538 | 0.92[ASN][1000 genomes] |
rs6828950 | 0.92[ASN][1000 genomes] |
rs6829477 | 0.81[ASN][1000 genomes] |
rs6831418 | 0.81[ASN][1000 genomes] |
rs6834911 | 0.85[ASN][1000 genomes] |
rs6835688 | 0.91[ASN][1000 genomes] |
rs6843053 | 0.91[ASN][1000 genomes] |
rs6847607 | 0.81[ASN][1000 genomes] |
rs6848017 | 0.89[ASN][1000 genomes] |
rs6851643 | 0.80[ASN][1000 genomes] |
rs6851987 | 0.81[ASN][1000 genomes] |
rs6854743 | 0.92[ASN][1000 genomes] |
rs6857888 | 0.87[ASN][1000 genomes] |
rs6858126 | 0.85[ASN][1000 genomes] |
rs6858132 | 0.85[ASN][1000 genomes] |
rs6858143 | 0.85[ASN][1000 genomes] |
rs6858333 | 0.87[ASN][1000 genomes] |
rs6858439 | 0.87[ASN][1000 genomes] |
rs6858699 | 0.87[ASN][1000 genomes] |
rs7654266 | 0.91[ASN][1000 genomes] |
rs7663201 | 0.83[ASN][1000 genomes] |
rs7663374 | 0.83[ASN][1000 genomes] |
rs7676033 | 0.91[ASN][1000 genomes] |
rs7691832 | 0.91[ASN][1000 genomes] |
rs7692197 | 0.91[ASN][1000 genomes] |
rs916876 | 0.91[ASN][1000 genomes] |
rs916877 | 0.91[ASN][1000 genomes] |
rs916878 | 0.91[ASN][1000 genomes] |
rs9307148 | 0.89[ASN][1000 genomes] |
rs978122 | 0.91[ASN][1000 genomes] |
rs9992130 | 0.91[ASN][1000 genomes] |
rs9995378 | 0.91[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv932216 | chr4:95501261-96109807 | Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
2 | nsv1003860 | chr4:95507683-96120619 | Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 8 gene(s) | inside rSNPs | diseases |
3 | nsv869528 | chr4:95537649-96368018 | Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
4 | nsv1005816 | chr4:95573444-95902704 | Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 8 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:95768800-95789600 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
2 | chr4:95769000-95789600 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
3 | chr4:95770200-95771200 | Enhancers | Thymus | Thymus |
4 | chr4:95770200-95771400 | Enhancers | Ganglion Eminence derived primary cultured neurospheres | brain |
5 | chr4:95770400-95771000 | Enhancers | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
6 | chr4:95770400-95771200 | Enhancers | Fetal Thymus | thymus |
7 | chr4:95770400-95771200 | Enhancers | Gastric | stomach |
8 | chr4:95770600-95771000 | Enhancers | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
9 | chr4:95770600-95771400 | Enhancers | Cortex derived primary cultured neurospheres | brain |
10 | chr4:95770800-95772200 | Enhancers | A549 | lung |