Variant report
Variant | rs9504009 |
---|---|
Chromosome Location | chr6:4255905-4255906 |
allele | C/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 | chr6:4252767..4255076-chr6:4255779..4258262,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10080414 | 0.88[EUR][1000 genomes] |
rs10223886 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs10428864 | 0.87[EUR][1000 genomes] |
rs1072903 | 0.88[EUR][1000 genomes] |
rs11756906 | 1.00[JPT][hapmap] |
rs11961149 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs11970375 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs11970430 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs1591412 | 0.89[EUR][1000 genomes] |
rs17500205 | 0.94[EUR][1000 genomes] |
rs17538963 | 0.80[EUR][1000 genomes] |
rs17565229 | 0.95[EUR][1000 genomes] |
rs1832060 | 0.89[EUR][1000 genomes] |
rs2210761 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs2210762 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs2326473 | 0.89[EUR][1000 genomes] |
rs4255019 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs4256473 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs4317452 | 0.80[EUR][1000 genomes] |
rs4354197 | 0.80[EUR][1000 genomes] |
rs4443539 | 0.98[EUR][1000 genomes] |
rs4475361 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs4526241 | 0.89[EUR][1000 genomes] |
rs4596533 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4629733 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4959937 | 0.88[EUR][1000 genomes] |
rs4959938 | 0.88[EUR][1000 genomes] |
rs57509474 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs58402712 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs59706955 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs60023788 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs61604146 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs6597046 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs6597047 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs6597048 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs6913742 | 0.89[EUR][1000 genomes] |
rs6916181 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs6922330 | 0.88[EUR][1000 genomes] |
rs6931784 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs6934489 | 0.90[EUR][1000 genomes] |
rs6934652 | 0.90[EUR][1000 genomes] |
rs73356806 | 0.80[EUR][1000 genomes] |
rs73358820 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs73358823 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs73358854 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs73360930 | 1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs73360933 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs73360945 | 0.99[EUR][1000 genomes] |
rs7754298 | 0.95[EUR][1000 genomes] |
rs7759565 | 0.88[EUR][1000 genomes] |
rs7763657 | 0.96[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs7763789 | 0.86[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7765457 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs913405 | 0.94[EUR][1000 genomes] |
rs9328227 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs9328229 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs9328230 | 0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs9328231 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs9328232 | 0.90[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs9328233 | 0.90[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs9328236 | 0.99[EUR][1000 genomes] |
rs9392032 | 0.90[EUR][1000 genomes] |
rs9392578 | 0.86[EUR][1000 genomes] |
rs9392580 | 0.88[EUR][1000 genomes] |
rs9405228 | 0.90[EUR][1000 genomes] |
rs9502148 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs9502149 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs9502150 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs9502151 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9502152 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9502153 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs9502154 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs9502157 | 0.99[EUR][1000 genomes] |
rs9502158 | 0.99[EUR][1000 genomes] |
rs9502159 | 0.99[EUR][1000 genomes] |
rs9502160 | 0.98[EUR][1000 genomes] |
rs9502161 | 0.93[EUR][1000 genomes] |
rs9502163 | 0.94[EUR][1000 genomes] |
rs9503948 | 0.80[EUR][1000 genomes] |
rs9503953 | 0.80[EUR][1000 genomes] |
rs9503982 | 0.89[EUR][1000 genomes] |
rs9503983 | 0.89[EUR][1000 genomes] |
rs9503984 | 0.89[EUR][1000 genomes] |
rs9503985 | 0.86[EUR][1000 genomes] |
rs9503993 | 0.96[EUR][1000 genomes] |
rs9503994 | 0.96[EUR][1000 genomes] |
rs9503995 | 0.96[EUR][1000 genomes] |
rs9503996 | 0.80[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs9504005 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs9504006 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs9504007 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9504008 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9504010 | 1.00[EUR][1000 genomes] |
rs9504022 | 0.99[EUR][1000 genomes] |
rs9504025 | 0.94[EUR][1000 genomes] |
rs9504033 | 0.95[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1022968 | chr6:3862744-4272502 | Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 56 gene(s) | inside rSNPs | diseases |
2 | nsv538106 | chr6:3862744-4272502 | Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 56 gene(s) | inside rSNPs | diseases |
3 | esv2422457 | chr6:4100333-4377396 | Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 34 gene(s) | inside rSNPs | diseases |
4 | nsv600861 | chr6:4238488-4469641 | Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
5 | nsv462618 | chr6:4238488-4472587 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
6 | nsv600862 | chr6:4238488-4472587 | Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
7 | nsv949364 | chr6:4253413-4466981 | Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
8 | esv17585 | chr6:4254023-4257185 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
9 | nsv600863 | chr6:4255387-4472587 | Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
10 | nsv1027498 | chr6:4255640-4471635 | Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
11 | esv2763995 | chr6:4255640-4474114 | Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
12 | nsv1020205 | chr6:4255640-4474114 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
13 | nsv600864 | chr6:4255708-4464630 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
14 | nsv516402 | chr6:4255708-4472587 | Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
15 | nsv462619 | chr6:4255708-4472587 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
16 | nsv600865 | chr6:4255708-4472587 | Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
17 | nsv462620 | chr6:4255708-4481421 | Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
18 | nsv600866 | chr6:4255708-4481421 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
19 | nsv600867 | chr6:4255725-4464630 | Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
20 | nsv462621 | chr6:4255725-4472587 | Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
21 | nsv600868 | chr6:4255725-4472587 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
22 | nsv1029501 | chr6:4255745-4471635 | Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
23 | nsv432845 | chr6:4255905-4471472 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:4254200-4259000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr6:4254400-4258000 | Weak transcription | Lung | lung |
3 | chr6:4254600-4256800 | Weak transcription | Placenta | Placenta |
4 | chr6:4254600-4258200 | Weak transcription | Left Ventricle | heart |
5 | chr6:4254600-4259600 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
6 | chr6:4254800-4256800 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
7 | chr6:4254800-4258200 | Weak transcription | Right Atrium | heart |
8 | chr6:4254800-4258800 | Weak transcription | NHEK | skin |
9 | chr6:4254800-4259000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
10 | chr6:4255000-4256800 | Weak transcription | HUVEC | blood vessel |
11 | chr6:4255400-4258400 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
12 | chr6:4255600-4256000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |