Variant report
Variant | rs11119415 |
---|---|
Chromosome Location | chr1:210306944-210306945 |
allele | C/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] |
---|---|
rs1040425 | 0.92[EUR][1000 genomes] |
rs10489346 | 1.00[CEU][hapmap];0.91[CHB][hapmap] |
rs10779521 | 1.00[CEU][hapmap];0.91[CHB][hapmap];0.83[JPT][hapmap];0.81[ASN][1000 genomes] |
rs10863800 | 1.00[CEU][hapmap];0.90[CHB][hapmap] |
rs11119403 | 0.81[ASN][1000 genomes] |
rs11119417 | 0.96[ASN][1000 genomes] |
rs11119419 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs11119420 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs11119445 | 1.00[CEU][hapmap] |
rs12061641 | 0.81[ASN][1000 genomes] |
rs12073617 | 0.81[ASN][1000 genomes] |
rs12079916 | 0.89[ASN][1000 genomes] |
rs12088422 | 0.84[ASN][1000 genomes] |
rs12089327 | 0.95[ASN][1000 genomes] |
rs12092527 | 0.94[ASN][1000 genomes] |
rs12406136 | 0.84[ASN][1000 genomes] |
rs12409047 | 0.94[ASN][1000 genomes] |
rs12566105 | 0.89[ASN][1000 genomes] |
rs17015667 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes] |
rs17015701 | 0.82[YRI][hapmap];0.80[AFR][1000 genomes] |
rs2151940 | 0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs4844509 | 0.89[ASN][1000 genomes] |
rs4844923 | 1.00[CEU][hapmap];0.86[CHB][hapmap] |
rs4844940 | 1.00[CEU][hapmap];0.91[CHB][hapmap];0.83[JPT][hapmap] |
rs4844941 | 0.81[ASN][1000 genomes] |
rs4844942 | 0.81[ASN][1000 genomes] |
rs4844944 | 0.80[ASN][1000 genomes] |
rs4844950 | 0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs4844955 | 0.94[JPT][hapmap];0.84[ASN][1000 genomes] |
rs646906 | 1.00[CEU][hapmap] |
rs713114 | 0.86[CHB][hapmap] |
rs72649937 | 0.81[ASN][1000 genomes] |
rs72649938 | 0.81[ASN][1000 genomes] |
rs72649940 | 0.81[ASN][1000 genomes] |
rs72649955 | 0.98[ASN][1000 genomes] |
rs72649956 | 0.84[ASN][1000 genomes] |
rs72649959 | 0.84[ASN][1000 genomes] |
rs72649960 | 0.84[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1014034 | chr1:209759648-210501731 | Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 45 gene(s) | inside rSNPs | diseases |
2 | nsv873140 | chr1:210068117-210335644 | Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
3 | nsv873144 | chr1:210252522-210347417 | Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
4 | nsv873145 | chr1:210302595-210347417 | Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
5 | nsv468072 | chr1:210304319-210338196 | Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
6 | nsv549104 | chr1:210304319-210338196 | Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
7 | nsv549105 | chr1:210304319-210338397 | Weak transcription ZNF genes & repeats Enhancers Genic enhancers Strong transcription | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:210298400-210318200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr1:210303400-210308200 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
3 | chr1:210305400-210318400 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |