Variant report
Variant | rs17178665 |
---|---|
Chromosome Location | chr6:29747011-29747012 |
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] |
---|---|
rs11751282 | 0.81[EUR][1000 genomes] |
rs11751381 | 0.81[EUR][1000 genomes] |
rs11751397 | 0.81[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs11751848 | 0.81[EUR][1000 genomes] |
rs11751915 | 0.81[EUR][1000 genomes] |
rs11752530 | 0.81[EUR][1000 genomes] |
rs11753758 | 0.81[EUR][1000 genomes] |
rs11753812 | 0.81[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs11753867 | 0.81[EUR][1000 genomes] |
rs11753872 | 0.81[EUR][1000 genomes] |
rs11754577 | 0.81[EUR][1000 genomes] |
rs11755659 | 0.81[EUR][1000 genomes] |
rs11757126 | 0.81[EUR][1000 genomes] |
rs11757182 | 0.81[EUR][1000 genomes] |
rs11757929 | 0.81[EUR][1000 genomes] |
rs11757937 | 0.81[EUR][1000 genomes] |
rs11757990 | 0.81[EUR][1000 genomes] |
rs11758056 | 0.81[EUR][1000 genomes] |
rs11758087 | 0.81[EUR][1000 genomes] |
rs11759271 | 0.81[EUR][1000 genomes] |
rs12110334 | 0.81[EUR][1000 genomes] |
rs12110682 | 0.81[EUR][1000 genomes] |
rs12111521 | 0.81[EUR][1000 genomes] |
rs17178224 | 0.86[EUR][1000 genomes] |
rs17178441 | 0.83[AFR][1000 genomes] |
rs17178602 | 0.98[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17178658 | 1.00[EUR][1000 genomes] |
rs17178735 | 0.81[EUR][1000 genomes] |
rs17178749 | 0.81[EUR][1000 genomes] |
rs17178826 | 0.81[EUR][1000 genomes] |
rs17178938 | 0.85[EUR][1000 genomes] |
rs17178989 | 0.85[EUR][1000 genomes] |
rs17184633 | 0.86[EUR][1000 genomes] |
rs17185244 | 0.81[EUR][1000 genomes] |
rs17185258 | 1.00[EUR][1000 genomes] |
rs17875375 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17875384 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17875387 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2272871 | 0.81[EUR][1000 genomes] |
rs2474100 | 0.86[EUR][1000 genomes] |
rs2535234 | 0.86[EUR][1000 genomes] |
rs2535241 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2535251 | 0.86[EUR][1000 genomes] |
rs2535252 | 0.86[EUR][1000 genomes] |
rs2535255 | 0.86[EUR][1000 genomes] |
rs2535256 | 0.86[EUR][1000 genomes] |
rs2535257 | 0.86[EUR][1000 genomes] |
rs2535259 | 0.86[EUR][1000 genomes] |
rs2747418 | 0.86[EUR][1000 genomes] |
rs2747419 | 0.86[EUR][1000 genomes] |
rs2747437 | 0.86[EUR][1000 genomes] |
rs2747439 | 0.86[EUR][1000 genomes] |
rs2747441 | 0.86[EUR][1000 genomes] |
rs2747444 | 0.86[EUR][1000 genomes] |
rs2747446 | 0.86[EUR][1000 genomes] |
rs2747450 | 0.86[EUR][1000 genomes] |
rs2747452 | 0.86[EUR][1000 genomes] |
rs2747459 | 0.86[EUR][1000 genomes] |
rs2747461 | 0.86[EUR][1000 genomes] |
rs2747462 | 0.86[EUR][1000 genomes] |
rs2747464 | 0.86[EUR][1000 genomes] |
rs2747465 | 0.86[EUR][1000 genomes] |
rs2747466 | 0.86[EUR][1000 genomes] |
rs2857768 | 0.86[EUR][1000 genomes] |
rs2857780 | 0.86[EUR][1000 genomes] |
rs2857783 | 0.86[EUR][1000 genomes] |
rs2857784 | 0.86[EUR][1000 genomes] |
rs28578751 | 0.81[EUR][1000 genomes] |
rs28802633 | 0.81[EUR][1000 genomes] |
rs28840978 | 0.81[EUR][1000 genomes] |
rs2894117 | 0.81[EUR][1000 genomes] |
rs2907893 | 0.86[EUR][1000 genomes] |
rs2907894 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2982835 | 0.86[EUR][1000 genomes] |
rs2982838 | 0.86[EUR][1000 genomes] |
rs2982840 | 0.86[EUR][1000 genomes] |
rs3094737 | 0.81[EUR][1000 genomes] |
rs3117288 | 1.00[EUR][1000 genomes] |
rs3117300 | 0.86[EUR][1000 genomes] |
rs3117302 | 0.86[EUR][1000 genomes] |
rs3117304 | 0.86[EUR][1000 genomes] |
rs3117305 | 0.81[EUR][1000 genomes] |
rs3117306 | 0.86[EUR][1000 genomes] |
rs3117307 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs3117308 | 0.86[EUR][1000 genomes] |
rs3117309 | 0.86[EUR][1000 genomes] |
rs3117310 | 0.86[EUR][1000 genomes] |
rs3117314 | 0.86[EUR][1000 genomes] |
rs3117316 | 0.86[EUR][1000 genomes] |
rs3129040 | 0.86[EUR][1000 genomes] |
rs3129050 | 0.86[EUR][1000 genomes] |
rs3129051 | 0.86[EUR][1000 genomes] |
rs3129186 | 0.86[EUR][1000 genomes] |
rs34416032 | 0.81[EUR][1000 genomes] |
rs34735344 | 0.81[EUR][1000 genomes] |
rs34792092 | 0.81[EUR][1000 genomes] |
rs35197595 | 0.81[EUR][1000 genomes] |
rs35728173 | 0.81[EUR][1000 genomes] |
rs35794939 | 0.81[EUR][1000 genomes] |
rs36073133 | 0.81[EUR][1000 genomes] |
rs36106954 | 0.81[EUR][1000 genomes] |
rs3734820 | 0.81[EUR][1000 genomes] |
rs385743 | 0.81[EUR][1000 genomes] |
rs387603 | 0.86[EUR][1000 genomes] |
rs3891162 | 0.81[EUR][1000 genomes] |
rs3892549 | 0.81[EUR][1000 genomes] |
rs3906248 | 0.81[EUR][1000 genomes] |
rs398931 | 0.86[EUR][1000 genomes] |
rs3998745 | 0.81[EUR][1000 genomes] |
rs406424 | 0.86[EUR][1000 genomes] |
rs4098859 | 0.81[EUR][1000 genomes] |
rs423281 | 0.86[EUR][1000 genomes] |
rs423369 | 0.86[EUR][1000 genomes] |
rs4409220 | 0.81[EUR][1000 genomes] |
rs56035102 | 0.81[EUR][1000 genomes] |
rs56091723 | 0.81[EUR][1000 genomes] |
rs56170912 | 1.00[EUR][1000 genomes] |
rs56182102 | 0.81[EUR][1000 genomes] |
rs56211519 | 0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56241766 | 0.81[EUR][1000 genomes] |
rs56315562 | 0.81[EUR][1000 genomes] |
rs58121457 | 0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58147175 | 0.81[EUR][1000 genomes] |
rs58449426 | 0.81[EUR][1000 genomes] |
rs59144130 | 0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59408697 | 0.81[EUR][1000 genomes] |
rs59416725 | 0.81[EUR][1000 genomes] |
rs59978815 | 0.81[EUR][1000 genomes] |
rs60299305 | 0.81[EUR][1000 genomes] |
rs61315420 | 0.81[EUR][1000 genomes] |
rs61524015 | 1.00[EUR][1000 genomes] |
rs6932033 | 0.81[EUR][1000 genomes] |
rs6932384 | 0.81[EUR][1000 genomes] |
rs72492263 | 0.81[EUR][1000 genomes] |
rs72507835 | 0.81[EUR][1000 genomes] |
rs72507839 | 0.81[EUR][1000 genomes] |
rs73745404 | 0.81[EUR][1000 genomes] |
rs73745405 | 0.81[EUR][1000 genomes] |
rs73745406 | 0.81[EUR][1000 genomes] |
rs73745429 | 0.81[EUR][1000 genomes] |
rs73745430 | 0.81[EUR][1000 genomes] |
rs73745431 | 0.81[EUR][1000 genomes] |
rs73745455 | 0.81[EUR][1000 genomes] |
rs73745456 | 0.81[EUR][1000 genomes] |
rs73745473 | 0.81[EUR][1000 genomes] |
rs73745480 | 0.97[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73745481 | 0.81[EUR][1000 genomes] |
rs73745483 | 0.81[EUR][1000 genomes] |
rs73745488 | 0.81[EUR][1000 genomes] |
rs73745489 | 0.81[EUR][1000 genomes] |
rs73745491 | 0.81[EUR][1000 genomes] |
rs73745492 | 0.81[EUR][1000 genomes] |
rs73745494 | 0.81[EUR][1000 genomes] |
rs73747518 | 0.81[EUR][1000 genomes] |
rs73747522 | 0.81[EUR][1000 genomes] |
rs73747524 | 0.81[EUR][1000 genomes] |
rs73747525 | 0.81[EUR][1000 genomes] |
rs73747534 | 0.81[EUR][1000 genomes] |
rs73747573 | 0.81[EUR][1000 genomes] |
rs73747576 | 0.81[EUR][1000 genomes] |
rs73747624 | 0.83[AFR][1000 genomes] |
rs7758742 | 0.81[EUR][1000 genomes] |
rs7763677 | 0.85[EUR][1000 genomes] |
rs7775919 | 0.81[EUR][1000 genomes] |
rs9468579 | 0.86[EUR][1000 genomes] |
rs9500984 | 0.81[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 | 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 | nsv508397 | chr6:29663132-29761448 | Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 26 gene(s) | inside rSNPs | diseases |
6 | 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 |
7 | 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 |
8 | 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 |
9 | 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 |
10 | 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 |
11 | 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 |
12 | 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 |
13 | 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 |
14 | 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 |
15 | 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 |
16 | 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 |
17 | nsv883536 | chr6:29746023-29760819 | Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
18 | 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 |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:29733600-29755800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
2 | chr6:29739000-29753600 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
3 | chr6:29745600-29747200 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
4 | chr6:29745600-29747200 | Enhancers | HUES6 Cell Line | embryonic stem cell |
5 | chr6:29746200-29747200 | Enhancers | HUES64 Cell Line | embryonic stem cell |
6 | chr6:29746400-29747200 | Enhancers | H9 Cell Line | embryonic stem cell |
7 | chr6:29746600-29747200 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
8 | chr6:29746800-29747200 | Enhancers | Primary T helper memory cells from peripheral blood 2 | blood |
9 | chr6:29747000-29748000 | Enhancers | Primary T helper cells fromperipheralblood | blood |