Variant report
Variant | rs10150789 |
---|---|
Chromosome Location | chr14:68536052-68536053 |
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 | chr14:68524998..68527629-chr14:68533348..68536338,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10130997 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10132711 | 0.91[AFR][1000 genomes] |
rs10134124 | 0.80[ASN][1000 genomes] |
rs10134320 | 0.80[ASN][1000 genomes] |
rs10134664 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs10135046 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs10135256 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs10137330 | 0.84[ASN][1000 genomes] |
rs10137457 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10137712 | 0.81[ASN][1000 genomes] |
rs10138719 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10140465 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs10142285 | 0.91[AFR][1000 genomes] |
rs10143895 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10144224 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs10145197 | 0.84[ASN][1000 genomes] |
rs10145820 | 0.91[AFR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs10146719 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10146766 | 0.89[AFR][1000 genomes] |
rs10146831 | 0.89[AFR][1000 genomes] |
rs10149801 | 0.80[ASN][1000 genomes] |
rs10150330 | 0.89[AFR][1000 genomes] |
rs10150584 | 0.84[ASN][1000 genomes] |
rs10151123 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10873211 | 0.84[ASN][1000 genomes] |
rs10873212 | 0.84[ASN][1000 genomes] |
rs11158710 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs11158720 | 0.92[ASN][1000 genomes] |
rs11158721 | 0.84[ASN][1000 genomes] |
rs11844842 | 0.84[ASN][1000 genomes] |
rs11847339 | 0.88[ASN][1000 genomes] |
rs11849196 | 0.84[ASN][1000 genomes] |
rs11851597 | 0.88[ASN][1000 genomes] |
rs11851991 | 0.94[ASN][1000 genomes] |
rs17104774 | 0.87[AFR][1000 genomes] |
rs17104783 | 0.89[AFR][1000 genomes] |
rs17104786 | 0.89[AFR][1000 genomes] |
rs17104824 | 0.91[AFR][1000 genomes] |
rs17104829 | 0.91[AFR][1000 genomes] |
rs17104862 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs17104863 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs17104880 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs17104900 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17104917 | 0.94[ASN][1000 genomes] |
rs17104947 | 0.84[ASN][1000 genomes] |
rs17104953 | 0.84[ASN][1000 genomes] |
rs17104992 | 0.84[ASN][1000 genomes] |
rs17105001 | 0.90[ASN][1000 genomes] |
rs1951411 | 0.84[ASN][1000 genomes] |
rs2057361 | 0.92[ASN][1000 genomes] |
rs2180537 | 0.87[AFR][1000 genomes] |
rs28372014 | 0.81[ASN][1000 genomes] |
rs28434770 | 0.87[AFR][1000 genomes] |
rs28448732 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs28516665 | 0.89[AFR][1000 genomes] |
rs28716846 | 0.90[ASN][1000 genomes] |
rs28757308 | 0.89[AFR][1000 genomes] |
rs28816808 | 0.89[AFR][1000 genomes] |
rs28869007 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs34370899 | 0.84[ASN][1000 genomes] |
rs4902534 | 0.87[AFR][1000 genomes] |
rs4902541 | 0.91[AFR][1000 genomes] |
rs4902548 | 0.88[ASN][1000 genomes] |
rs60562079 | 0.88[ASN][1000 genomes] |
rs60841871 | 0.84[ASN][1000 genomes] |
rs6573802 | 0.86[AFR][1000 genomes] |
rs6573806 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs7140987 | 0.91[AFR][1000 genomes] |
rs7145089 | 0.88[ASN][1000 genomes] |
rs7147296 | 0.87[AFR][1000 genomes] |
rs7147522 | 0.84[ASN][1000 genomes] |
rs7147935 | 0.80[ASN][1000 genomes] |
rs7148799 | 0.84[ASN][1000 genomes] |
rs7149343 | 0.88[ASN][1000 genomes] |
rs7149460 | 0.89[AFR][1000 genomes] |
rs7150716 | 0.84[ASN][1000 genomes] |
rs7153470 | 0.89[AFR][1000 genomes] |
rs7153978 | 0.88[ASN][1000 genomes] |
rs7154228 | 0.88[ASN][1000 genomes] |
rs7154645 | 0.88[ASN][1000 genomes] |
rs7154725 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7155152 | 0.88[ASN][1000 genomes] |
rs7157152 | 0.84[ASN][1000 genomes] |
rs7157550 | 0.91[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs7157720 | 0.89[AFR][1000 genomes] |
rs7160068 | 0.84[ASN][1000 genomes] |
rs7161070 | 0.90[ASN][1000 genomes] |
rs73286292 | 0.84[ASN][1000 genomes] |
rs7359083 | 0.94[ASN][1000 genomes] |
rs8003181 | 0.84[AFR][1000 genomes] |
rs8007347 | 0.90[ASN][1000 genomes] |
rs8008413 | 0.88[ASN][1000 genomes] |
rs8011367 | 0.84[ASN][1000 genomes] |
rs8012493 | 0.80[ASN][1000 genomes] |
rs8013061 | 0.84[ASN][1000 genomes] |
rs8014844 | 0.89[AFR][1000 genomes] |
rs8015741 | 0.88[AFR][1000 genomes] |
rs8018029 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs957930 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs9652364 | 0.89[AFR][1000 genomes] |
rs9672111 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv869154 | chr14:68366754-69041768 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:68532400-68536200 | Weak transcription | Gastric | stomach |
2 | chr14:68532400-68544000 | Weak transcription | Aorta | Aorta |
3 | chr14:68532400-68552400 | Weak transcription | Ovary | ovary |
4 | chr14:68534600-68536200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |