Variant report
Variant | rs16895757 |
---|---|
Chromosome Location | chr6:29762178-29762179 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
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(count:2 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs17179010 | 0.83[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs17179017 | 0.88[ASN][1000 genomes] |
rs17179038 | 0.88[ASN][1000 genomes] |
rs17179066 | 0.88[ASN][1000 genomes] |
rs17179101 | 0.83[AMR][1000 genomes];0.85[ASN][1000 genomes] |
rs17184661 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs17185419 | 0.83[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs17185426 | 0.83[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs17185440 | 0.88[ASN][1000 genomes] |
rs17185447 | 0.88[ASN][1000 genomes] |
rs2394172 | 0.89[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs3888722 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs3906306 | 1.00[AFR][1000 genomes] |
rs4085262 | 1.00[AFR][1000 genomes] |
rs4085264 | 1.00[AFR][1000 genomes] |
rs4143366 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs55661776 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs55672647 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs55693745 | 1.00[AFR][1000 genomes] |
rs55729140 | 0.88[ASN][1000 genomes] |
rs55791644 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs55792521 | 0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs55882115 | 1.00[AFR][1000 genomes] |
rs55884048 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs55933609 | 1.00[AFR][1000 genomes] |
rs55947552 | 1.00[AFR][1000 genomes] |
rs55970611 | 0.88[ASN][1000 genomes] |
rs56044823 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs56101454 | 1.00[AFR][1000 genomes] |
rs56104249 | 1.00[AMR][1000 genomes];0.88[ASN][1000 genomes] |
rs56128518 | 0.83[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs56155978 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs56172386 | 1.00[AFR][1000 genomes] |
rs56174454 | 1.00[AFR][1000 genomes] |
rs56236016 | 0.83[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs56269224 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs56287651 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs56290866 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs56324548 | 0.88[ASN][1000 genomes] |
rs56353080 | 1.00[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs56392172 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs58075773 | 0.92[AMR][1000 genomes];0.88[ASN][1000 genomes] |
rs61609080 | 0.92[AMR][1000 genomes];0.88[ASN][1000 genomes] |
rs62389314 | 1.00[AFR][1000 genomes] |
rs62389318 | 1.00[AFR][1000 genomes];0.85[AMR][1000 genomes] |
rs62389327 | 1.00[AFR][1000 genomes];0.85[AMR][1000 genomes] |
rs62389328 | 1.00[AFR][1000 genomes];0.85[AMR][1000 genomes] |
rs62389329 | 1.00[AFR][1000 genomes];0.85[AMR][1000 genomes] |
rs62389356 | 1.00[AFR][1000 genomes] |
rs62391766 | 1.00[AFR][1000 genomes] |
rs62391767 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62391768 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62391770 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62391785 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs62391786 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62391801 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs62391819 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs62391821 | 0.95[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs62391822 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs62391833 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs62391835 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs62391842 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs62391843 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs62391844 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs62391850 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs62391851 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs62391962 | 0.83[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs62391963 | 0.83[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs62391965 | 0.83[AMR][1000 genomes];0.88[ASN][1000 genomes] |
rs62392949 | 1.00[AFR][1000 genomes] |
rs62392950 | 1.00[AFR][1000 genomes] |
rs62392953 | 1.00[AFR][1000 genomes] |
rs62392954 | 1.00[AFR][1000 genomes] |
rs62392955 | 1.00[AFR][1000 genomes] |
rs62392956 | 1.00[AFR][1000 genomes] |
rs62392957 | 1.00[AFR][1000 genomes] |
rs62392958 | 1.00[AFR][1000 genomes] |
rs62394668 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs62394669 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs62394670 | 1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs62394676 | 1.00[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs62394678 | 1.00[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs62394681 | 0.83[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs62394682 | 0.88[ASN][1000 genomes] |
rs67382831 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs71550159 | 1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][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 | nsv428475 | chr6:29659525-29763392 | Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 27 gene(s) | inside rSNPs | diseases |
3 | 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 |
4 | 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 |
5 | esv1794141 | chr6:29670915-29765814 | Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 28 gene(s) | inside rSNPs | diseases |
6 | 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 |
7 | 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 |
8 | 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 |
9 | 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 |
10 | 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 |
11 | 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 |
12 | 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 |
13 | 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 |
14 | 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 |
15 | 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 |
16 | nsv883537 | chr6:29746023-29767611 | Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
17 | 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 |
18 | 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 |
19 | 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 |
20 | 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 |
21 | 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 |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:29760400-29764400 | Weak transcription | Hela-S3 | cervix |
2 | chr6:29761000-29763000 | Enhancers | Foreskin Melanocyte Primary Cells skin01 | Skin |
3 | chr6:29761000-29765200 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
4 | chr6:29761200-29762200 | Strong transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
5 | chr6:29761200-29763800 | Weak transcription | HMEC | breast |
6 | chr6:29761200-29763800 | Weak transcription | NHEK | skin |
7 | chr6:29761200-29764400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
8 | chr6:29761400-29763800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
9 | chr6:29761800-29766200 | Weak transcription | Pancreas | Pancrea |