Variant report
Variant | rs11118817 |
---|---|
Chromosome Location | chr1:221851582-221851583 |
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] |
---|---|
rs10429944 | 0.87[ASN][1000 genomes] |
rs10429945 | 0.87[ASN][1000 genomes] |
rs10429946 | 0.87[ASN][1000 genomes] |
rs10429956 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10429957 | 0.90[ASN][1000 genomes] |
rs10429958 | 0.90[ASN][1000 genomes] |
rs10429960 | 0.87[ASN][1000 genomes] |
rs10429961 | 0.90[ASN][1000 genomes] |
rs10429963 | 0.87[ASN][1000 genomes] |
rs10429964 | 0.87[ASN][1000 genomes] |
rs10495165 | 0.81[EUR][1000 genomes] |
rs10495166 | 0.81[EUR][1000 genomes] |
rs10495167 | 0.81[EUR][1000 genomes] |
rs10495168 | 0.81[EUR][1000 genomes] |
rs10863644 | 0.90[ASN][1000 genomes] |
rs10863645 | 0.90[ASN][1000 genomes] |
rs10863646 | 0.87[ASN][1000 genomes] |
rs11118748 | 0.81[EUR][1000 genomes] |
rs11118802 | 0.85[ASN][1000 genomes] |
rs11118806 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs11118807 | 0.85[ASN][1000 genomes] |
rs11118808 | 0.85[ASN][1000 genomes] |
rs11118809 | 0.85[ASN][1000 genomes] |
rs11118810 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs11118811 | 0.85[ASN][1000 genomes] |
rs11118812 | 0.90[ASN][1000 genomes] |
rs11118813 | 0.90[ASN][1000 genomes] |
rs11118814 | 0.90[ASN][1000 genomes] |
rs11118815 | 0.90[ASN][1000 genomes] |
rs11118816 | 0.90[ASN][1000 genomes] |
rs11118818 | 0.90[ASN][1000 genomes] |
rs11118819 | 0.90[ASN][1000 genomes] |
rs11118821 | 0.90[ASN][1000 genomes] |
rs11576646 | 0.90[ASN][1000 genomes] |
rs11587933 | 0.81[ASN][1000 genomes] |
rs11808469 | 0.90[ASN][1000 genomes] |
rs11808503 | 0.90[ASN][1000 genomes] |
rs11809184 | 0.90[ASN][1000 genomes] |
rs11809818 | 0.90[ASN][1000 genomes] |
rs11810697 | 0.90[ASN][1000 genomes] |
rs11811485 | 0.90[ASN][1000 genomes] |
rs11811644 | 0.90[ASN][1000 genomes] |
rs12021627 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs12021952 | 1.00[AFR][1000 genomes];0.88[EUR][1000 genomes] |
rs12023345 | 0.90[ASN][1000 genomes] |
rs12024440 | 0.90[ASN][1000 genomes] |
rs12024464 | 0.90[ASN][1000 genomes] |
rs12025710 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs12025878 | 0.90[ASN][1000 genomes] |
rs12027038 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs12031670 | 0.90[ASN][1000 genomes] |
rs12035928 | 0.85[ASN][1000 genomes] |
rs12036305 | 0.85[ASN][1000 genomes] |
rs12036766 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs12036771 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12037629 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12037802 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12041614 | 0.90[ASN][1000 genomes] |
rs12042290 | 0.90[ASN][1000 genomes] |
rs12043339 | 0.97[ASN][1000 genomes] |
rs12044981 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12401793 | 1.00[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs12403055 | 0.81[EUR][1000 genomes] |
rs12403320 | 1.00[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs12404274 | 0.81[EUR][1000 genomes] |
rs12405504 | 0.81[EUR][1000 genomes] |
rs12406074 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12406778 | 1.00[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs12407358 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12408488 | 0.85[ASN][1000 genomes] |
rs12408495 | 0.85[ASN][1000 genomes] |
rs12409206 | 0.81[EUR][1000 genomes] |
rs12409261 | 1.00[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs12409984 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.88[EUR][1000 genomes] |
rs12410562 | 0.81[EUR][1000 genomes] |
rs12411238 | 0.81[EUR][1000 genomes] |
rs13375747 | 0.90[ASN][1000 genomes] |
rs13375841 | 0.90[ASN][1000 genomes] |
rs13376168 | 0.88[ASN][1000 genomes] |
rs13376174 | 0.90[ASN][1000 genomes] |
rs13376254 | 0.90[ASN][1000 genomes] |
rs13376595 | 0.90[ASN][1000 genomes] |
rs1519464 | 0.90[ASN][1000 genomes] |
rs1519465 | 0.90[ASN][1000 genomes] |
rs17010272 | 0.81[EUR][1000 genomes] |
rs17010290 | 1.00[AFR][1000 genomes];0.85[EUR][1000 genomes] |
rs17010309 | 1.00[AFR][1000 genomes];0.85[EUR][1000 genomes] |
rs17010459 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs17010465 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs17010479 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs17010482 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs17010588 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs17041848 | 1.00[AFR][1000 genomes];0.85[EUR][1000 genomes] |
rs17041852 | 0.81[EUR][1000 genomes] |
rs17041853 | 0.81[EUR][1000 genomes] |
rs1850831 | 0.90[ASN][1000 genomes] |
rs1914947 | 0.85[ASN][1000 genomes] |
rs1949508 | 0.85[ASN][1000 genomes] |
rs2056289 | 0.83[ASN][1000 genomes] |
rs34494638 | 0.90[ASN][1000 genomes] |
rs4465212 | 0.85[ASN][1000 genomes] |
rs58002157 | 0.81[EUR][1000 genomes] |
rs58467896 | 0.81[EUR][1000 genomes] |
rs58516053 | 0.81[EUR][1000 genomes] |
rs58659812 | 0.81[EUR][1000 genomes] |
rs58696164 | 0.81[EUR][1000 genomes] |
rs58897885 | 0.90[ASN][1000 genomes] |
rs60436564 | 0.90[ASN][1000 genomes] |
rs61817912 | 0.85[ASN][1000 genomes] |
rs61817913 | 0.85[ASN][1000 genomes] |
rs61817924 | 0.90[ASN][1000 genomes] |
rs61817926 | 0.90[ASN][1000 genomes] |
rs61817941 | 0.90[ASN][1000 genomes] |
rs61817945 | 0.90[ASN][1000 genomes] |
rs61817946 | 0.90[ASN][1000 genomes] |
rs61817947 | 0.90[ASN][1000 genomes] |
rs61817948 | 0.90[ASN][1000 genomes] |
rs6661401 | 0.90[ASN][1000 genomes] |
rs6686877 | 0.85[ASN][1000 genomes] |
rs6700504 | 0.95[ASN][1000 genomes] |
rs73106612 | 0.81[EUR][1000 genomes] |
rs73106614 | 0.81[EUR][1000 genomes] |
rs73106616 | 0.81[EUR][1000 genomes] |
rs73106619 | 0.81[EUR][1000 genomes] |
rs73106624 | 0.81[EUR][1000 genomes] |
rs73106634 | 0.81[EUR][1000 genomes] |
rs73116215 | 0.81[EUR][1000 genomes] |
rs73116221 | 0.81[EUR][1000 genomes] |
rs73117996 | 0.81[EUR][1000 genomes] |
rs73117998 | 0.81[EUR][1000 genomes] |
rs73118002 | 0.81[EUR][1000 genomes] |
rs73119903 | 0.81[EUR][1000 genomes] |
rs73119916 | 0.81[EUR][1000 genomes] |
rs73119926 | 0.81[EUR][1000 genomes] |
rs73119928 | 0.81[EUR][1000 genomes] |
rs73119929 | 0.81[EUR][1000 genomes] |
rs73119932 | 0.81[EUR][1000 genomes] |
rs73119935 | 0.81[EUR][1000 genomes] |
rs73119938 | 0.81[EUR][1000 genomes] |
rs73119939 | 0.81[EUR][1000 genomes] |
rs73119945 | 0.81[EUR][1000 genomes] |
rs73119947 | 0.81[EUR][1000 genomes] |
rs73119948 | 0.81[EUR][1000 genomes] |
rs7417317 | 0.90[ASN][1000 genomes] |
rs7517462 | 0.90[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv997685 | chr1:220993527-221863416 | Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 28 gene(s) | inside rSNPs | diseases |
2 | nsv535299 | chr1:220993527-221863416 | Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 28 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:221846000-221861000 | Weak transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
2 | chr1:221846000-221869400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |