Variant report
Variant | rs11029138 |
---|---|
Chromosome Location | chr11:26103090-26103091 |
allele | A/C/G/T |
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] |
---|---|
rs10501037 | 1.00[ASN][1000 genomes] |
rs10734366 | 1.00[CHB][hapmap] |
rs10742127 | 1.00[CHB][hapmap] |
rs10742128 | 1.00[CHB][hapmap] |
rs10834897 | 1.00[CHB][hapmap] |
rs10834898 | 1.00[CHB][hapmap] |
rs11029104 | 0.84[EUR][1000 genomes] |
rs11029106 | 0.84[EUR][1000 genomes] |
rs11029114 | 1.00[CHB][hapmap] |
rs11029115 | 0.84[EUR][1000 genomes] |
rs11029120 | 0.82[ASN][1000 genomes] |
rs11029124 | 0.84[EUR][1000 genomes] |
rs11029127 | 1.00[ASN][1000 genomes] |
rs11029128 | 1.00[ASN][1000 genomes] |
rs11029130 | 1.00[ASN][1000 genomes] |
rs11029132 | 0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029133 | 1.00[ASN][1000 genomes] |
rs11029136 | 0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029137 | 1.00[ASN][1000 genomes] |
rs11029139 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029140 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029142 | 1.00[ASN][1000 genomes] |
rs11029143 | 1.00[ASN][1000 genomes] |
rs11029144 | 1.00[ASN][1000 genomes] |
rs11029145 | 1.00[ASN][1000 genomes] |
rs11029146 | 1.00[ASN][1000 genomes] |
rs11029147 | 1.00[ASN][1000 genomes] |
rs11029148 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029149 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029150 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029151 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029152 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029153 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029154 | 1.00[ASN][1000 genomes] |
rs11029155 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029156 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029157 | 1.00[ASN][1000 genomes] |
rs11029158 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029159 | 0.84[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029160 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029161 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029162 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029163 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029164 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029165 | 0.82[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029166 | 1.00[ASN][1000 genomes] |
rs11029167 | 1.00[ASN][1000 genomes] |
rs11029168 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029169 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029170 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029171 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029172 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029173 | 1.00[ASN][1000 genomes] |
rs11029174 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029175 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029176 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029177 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029178 | 1.00[ASN][1000 genomes] |
rs11029183 | 0.88[AFR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029184 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029185 | 0.88[AFR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029188 | 0.92[ASN][1000 genomes] |
rs11029189 | 1.00[ASN][1000 genomes] |
rs11029190 | 1.00[ASN][1000 genomes] |
rs11029191 | 1.00[ASN][1000 genomes] |
rs11029192 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029194 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029195 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029196 | 1.00[ASN][1000 genomes] |
rs11029197 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029198 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029199 | 1.00[ASN][1000 genomes] |
rs11029200 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029201 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029203 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029204 | 1.00[ASN][1000 genomes] |
rs11029205 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029210 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11029243 | 0.82[ASN][1000 genomes] |
rs11029244 | 0.82[ASN][1000 genomes] |
rs11029370 | 1.00[CEU][hapmap] |
rs11029371 | 1.00[CEU][hapmap] |
rs12222395 | 0.85[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs12222406 | 0.92[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs12223917 | 0.92[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs12224552 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12225865 | 1.00[CHB][hapmap] |
rs1387490 | 1.00[ASN][1000 genomes] |
rs1387491 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1387492 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1387503 | 1.00[CHB][hapmap] |
rs1387507 | 1.00[CHB][hapmap] |
rs1489508 | 0.82[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs1489509 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs1489510 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs1489511 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs16915262 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs16915268 | 1.00[ASN][1000 genomes] |
rs2349610 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2349611 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4360660 | 0.82[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs4572089 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs59456245 | 1.00[ASN][1000 genomes] |
rs61688636 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs6484193 | 1.00[CHB][hapmap] |
rs66633054 | 1.00[ASN][1000 genomes] |
rs66648383 | 1.00[ASN][1000 genomes] |
rs66699863 | 1.00[ASN][1000 genomes] |
rs7101817 | 1.00[CHB][hapmap] |
rs7105188 | 1.00[CHB][hapmap] |
rs7105339 | 1.00[CHB][hapmap] |
rs7115939 | 1.00[CHB][hapmap] |
rs7116083 | 1.00[CHB][hapmap] |
rs7119696 | 1.00[CHB][hapmap] |
rs7123678 | 1.00[CHB][hapmap] |
rs72885762 | 1.00[ASN][1000 genomes] |
rs73435407 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs73435414 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs73435415 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs73435418 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs73435435 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs73435438 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs73435442 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs73435450 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs73435451 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs73435502 | 0.88[AFR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7935278 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs7935406 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs7938817 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs7952271 | 0.80[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs9633820 | 1.00[ASN][1000 genomes] |
rs9633821 | 1.00[ASN][1000 genomes] |
rs9633854 | 1.00[ASN][1000 genomes] |
rs9633855 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs977800 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs988513 | 1.00[CHB][hapmap] |
rs988514 | 1.00[CHB][hapmap] |
rs988516 | 1.00[CHB][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2760599 | chr11:25186984-26159450 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | nsv1046507 | chr11:25469712-26111707 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:26101200-26109200 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
2 | chr11:26101400-26112600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr11:26101800-26103200 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
4 | chr11:26102000-26106200 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
5 | chr11:26102200-26109600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
6 | chr11:26102400-26106400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |