Variant report
Variant | rs1632980 |
---|---|
Chromosome Location | chr6:29773720-29773721 |
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] |
---|---|
rs1077433 | 0.82[EUR][1000 genomes] |
rs1079599 | 0.82[EUR][1000 genomes] |
rs1111673 | 0.82[EUR][1000 genomes] |
rs1318083 | 0.82[EUR][1000 genomes] |
rs1610641 | 0.81[EUR][1000 genomes] |
rs1610642 | 0.81[EUR][1000 genomes] |
rs1610648 | 0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs1610649 | 0.90[AFR][1000 genomes] |
rs1610650 | 0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs1610651 | 0.86[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1610653 | 0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs1610654 | 0.87[EUR][1000 genomes] |
rs1610655 | 0.88[EUR][1000 genomes] |
rs1610656 | 0.86[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs1610658 | 0.89[EUR][1000 genomes] |
rs1610659 | 0.89[EUR][1000 genomes] |
rs1610661 | 0.89[EUR][1000 genomes] |
rs1610662 | 0.85[EUR][1000 genomes] |
rs1610665 | 0.87[EUR][1000 genomes] |
rs1610669 | 0.85[ASN][1000 genomes] |
rs1610670 | 0.80[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs1610673 | 0.81[EUR][1000 genomes] |
rs1610697 | 0.87[EUR][1000 genomes] |
rs1610698 | 0.87[EUR][1000 genomes] |
rs1610700 | 0.80[EUR][1000 genomes] |
rs1610701 | 0.86[ASN][1000 genomes] |
rs1610703 | 0.86[ASN][1000 genomes] |
rs1610709 | 0.83[EUR][1000 genomes] |
rs1610710 | 0.87[EUR][1000 genomes] |
rs1610711 | 0.88[EUR][1000 genomes] |
rs1610712 | 0.86[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1610713 | 0.91[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1610714 | 0.88[EUR][1000 genomes] |
rs1610715 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs1610716 | 0.86[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs1610717 | 0.81[EUR][1000 genomes] |
rs1610722 | 0.81[EUR][1000 genomes] |
rs1610723 | 0.81[EUR][1000 genomes] |
rs1610724 | 0.81[EUR][1000 genomes] |
rs1610726 | 0.83[EUR][1000 genomes] |
rs1611172 | 0.85[EUR][1000 genomes] |
rs1611175 | 0.84[EUR][1000 genomes] |
rs1611178 | 0.86[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1611180 | 0.81[EUR][1000 genomes] |
rs1611184 | 0.81[EUR][1000 genomes] |
rs1611191 | 0.89[EUR][1000 genomes] |
rs1611193 | 0.86[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1611194 | 0.86[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1611195 | 0.89[EUR][1000 genomes] |
rs1611199 | 0.81[EUR][1000 genomes] |
rs1611200 | 0.81[EUR][1000 genomes] |
rs1611213 | 0.81[EUR][1000 genomes] |
rs1611218 | 0.81[EUR][1000 genomes] |
rs1611222 | 0.81[EUR][1000 genomes] |
rs1611228 | 0.82[EUR][1000 genomes] |
rs1611252 | 0.84[EUR][1000 genomes] |
rs1611260 | 0.82[EUR][1000 genomes] |
rs1611267 | 0.85[EUR][1000 genomes] |
rs1614309 | 0.84[EUR][1000 genomes] |
rs1615839 | 0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs1618670 | 0.81[EUR][1000 genomes] |
rs1620173 | 0.80[EUR][1000 genomes] |
rs1624302 | 0.90[EUR][1000 genomes] |
rs1629068 | 0.83[EUR][1000 genomes] |
rs1630969 | 0.83[EUR][1000 genomes] |
rs1632973 | 0.87[EUR][1000 genomes] |
rs1632976 | 0.87[EUR][1000 genomes] |
rs1632979 | 0.87[EUR][1000 genomes] |
rs1632981 | 0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1632982 | 0.88[AFR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs1632983 | 0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1632987 | 0.90[EUR][1000 genomes] |
rs1632988 | 0.88[EUR][1000 genomes] |
rs1632995 | 0.86[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1632996 | 0.86[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1632997 | 0.83[EUR][1000 genomes] |
rs1633000 | 0.82[EUR][1000 genomes] |
rs1633001 | 0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs1633002 | 0.83[EUR][1000 genomes] |
rs1633003 | 0.85[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1633004 | 0.83[EUR][1000 genomes] |
rs1633006 | 0.82[EUR][1000 genomes] |
rs1633007 | 0.85[EUR][1000 genomes] |
rs1633010 | 0.84[EUR][1000 genomes] |
rs1633014 | 0.84[EUR][1000 genomes] |
rs1633016 | 0.84[EUR][1000 genomes] |
rs1633018 | 0.83[EUR][1000 genomes] |
rs1633019 | 0.80[EUR][1000 genomes] |
rs1633020 | 0.83[EUR][1000 genomes] |
rs1633028 | 0.84[EUR][1000 genomes] |
rs1633030 | 0.84[EUR][1000 genomes] |
rs1633032 | 0.84[EUR][1000 genomes] |
rs1633033 | 0.84[EUR][1000 genomes] |
rs1633034 | 0.81[EUR][1000 genomes] |
rs1633035 | 0.81[EUR][1000 genomes] |
rs1736955 | 0.82[EUR][1000 genomes] |
rs1736958 | 0.82[EUR][1000 genomes] |
rs1736959 | 0.82[EUR][1000 genomes] |
rs1736963 | 0.86[EUR][1000 genomes] |
rs1736964 | 0.87[EUR][1000 genomes] |
rs1736966 | 0.87[EUR][1000 genomes] |
rs1736967 | 0.87[EUR][1000 genomes] |
rs1736968 | 0.87[EUR][1000 genomes] |
rs1736969 | 0.87[EUR][1000 genomes] |
rs1736971 | 0.87[EUR][1000 genomes] |
rs1736972 | 0.87[EUR][1000 genomes] |
rs1736973 | 0.87[EUR][1000 genomes] |
rs1736974 | 0.87[EUR][1000 genomes] |
rs1736975 | 0.87[EUR][1000 genomes] |
rs1736976 | 0.88[AFR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1736977 | 0.86[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs1736983 | 0.88[EUR][1000 genomes] |
rs1736984 | 0.86[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs1736985 | 0.88[EUR][1000 genomes] |
rs1736986 | 0.85[EUR][1000 genomes] |
rs1736991 | 0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1736998 | 0.82[EUR][1000 genomes] |
rs1736999 | 0.85[AFR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1737000 | 0.85[EUR][1000 genomes] |
rs1737003 | 0.81[EUR][1000 genomes] |
rs1737029 | 0.82[EUR][1000 genomes] |
rs1737031 | 0.83[EUR][1000 genomes] |
rs1737036 | 0.83[EUR][1000 genomes] |
rs1737038 | 0.83[EUR][1000 genomes] |
rs1737042 | 0.83[EUR][1000 genomes] |
rs1737047 | 0.82[EUR][1000 genomes] |
rs1737049 | 0.83[EUR][1000 genomes] |
rs2248870 | 0.87[EUR][1000 genomes] |
rs2248871 | 0.87[EUR][1000 genomes] |
rs2517919 | 0.84[EUR][1000 genomes] |
rs2517920 | 0.84[EUR][1000 genomes] |
rs2517921 | 0.86[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs2523410 | 0.85[EUR][1000 genomes] |
rs2735029 | 0.87[EUR][1000 genomes] |
rs2735042 | 0.83[EUR][1000 genomes] |
rs28514417 | 0.82[EUR][1000 genomes] |
rs2893981 | 0.82[EUR][1000 genomes] |
rs3129185 | 0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs739780 | 0.86[ASN][1000 genomes] |
rs753544 | 0.80[EUR][1000 genomes] |
rs885937 | 0.86[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs909720 | 0.85[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs909722 | 0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs9258448 | 0.87[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv20940 | chr6:29653954-29923410 | Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 46 gene(s) | inside rSNPs | diseases |
2 | nsv428139 | chr6:29659525-29892317 | Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 41 gene(s) | inside rSNPs | diseases |
3 | nsv427749 | chr6:29659525-29975144 | Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 53 gene(s) | inside rSNPs | diseases |
4 | nsv10809 | chr6:29692573-29794119 | Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 26 gene(s) | inside rSNPs | diseases |
5 | nsv883532 | chr6:29703262-29814963 | Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
6 | esv3441842 | chr6:29715749-29942950 | Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 47 gene(s) | inside rSNPs | diseases |
7 | esv11180 | chr6:29729381-29800066 | Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
8 | esv3332677 | chr6:29733187-29961463 | Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 43 gene(s) | inside rSNPs | diseases |
9 | esv3423001 | chr6:29733216-29878601 | Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 32 gene(s) | inside rSNPs | diseases |
10 | esv3475027 | chr6:29733297-29922699 | Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
11 | esv3475028 | chr6:29733297-29922699 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
12 | esv3420260 | chr6:29734457-29835593 | Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
13 | esv3330285 | chr6:29736281-29881328 | Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 31 gene(s) | inside rSNPs | diseases |
14 | nsv883539 | chr6:29748206-29780529 | Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
15 | esv3396224 | chr6:29754243-29888093 | Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 30 gene(s) | inside rSNPs | diseases |
16 | nsv965702 | chr6:29758408-29798943 | Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
17 | esv3430372 | chr6:29759523-29974277 | Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 42 gene(s) | inside rSNPs | diseases |
18 | esv3426050 | chr6:29761594-29918407 | Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 34 gene(s) | inside rSNPs | diseases |
19 | esv3431350 | chr6:29765473-29922767 | Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 34 gene(s) | inside rSNPs | diseases |
20 | nsv883540 | chr6:29772395-29784317 | Weak transcription Enhancers Bivalent Enhancer | TF binding regionChromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:29764800-29780600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |