Variant report
Variant | rs17014350 |
---|---|
Chromosome Location | chr12:87445622-87445623 |
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] |
---|---|
rs10858556 | 1.00[ASN][1000 genomes] |
rs11104222 | 1.00[ASN][1000 genomes] |
rs11104241 | 1.00[ASN][1000 genomes] |
rs11104353 | 1.00[ASN][1000 genomes] |
rs11608450 | 1.00[ASN][1000 genomes] |
rs11608474 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11608923 | 0.92[ASN][1000 genomes] |
rs11609545 | 1.00[ASN][1000 genomes] |
rs11610202 | 1.00[ASN][1000 genomes] |
rs11610240 | 1.00[ASN][1000 genomes] |
rs11610610 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11612996 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11613608 | 1.00[ASN][1000 genomes] |
rs11614902 | 1.00[ASN][1000 genomes] |
rs11615328 | 1.00[ASN][1000 genomes] |
rs12099694 | 1.00[ASN][1000 genomes] |
rs12099773 | 1.00[ASN][1000 genomes] |
rs12099774 | 1.00[ASN][1000 genomes] |
rs12301215 | 1.00[ASN][1000 genomes] |
rs12813003 | 0.92[ASN][1000 genomes] |
rs17014297 | 1.00[AMR][1000 genomes] |
rs17014343 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs17014345 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs17014347 | 0.84[ASN][1000 genomes] |
rs17014352 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs17014355 | 1.00[ASN][1000 genomes] |
rs17014357 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs17014359 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs17014361 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs17014363 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs17014366 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs17014369 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs17014430 | 1.00[ASN][1000 genomes] |
rs17040813 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs28438801 | 1.00[ASN][1000 genomes] |
rs34546765 | 0.92[ASN][1000 genomes] |
rs35212803 | 0.92[ASN][1000 genomes] |
rs35316438 | 0.92[ASN][1000 genomes] |
rs35772317 | 1.00[ASN][1000 genomes] |
rs55676823 | 1.00[ASN][1000 genomes] |
rs55742281 | 1.00[ASN][1000 genomes] |
rs55778807 | 1.00[ASN][1000 genomes] |
rs56212508 | 1.00[ASN][1000 genomes] |
rs58636507 | 0.91[ASN][1000 genomes] |
rs59432611 | 1.00[ASN][1000 genomes] |
rs59500185 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs60530487 | 1.00[ASN][1000 genomes] |
rs60718562 | 1.00[ASN][1000 genomes] |
rs61619114 | 1.00[ASN][1000 genomes] |
rs61951460 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs66473769 | 1.00[ASN][1000 genomes] |
rs66489945 | 1.00[ASN][1000 genomes] |
rs66507120 | 1.00[ASN][1000 genomes] |
rs66520580 | 1.00[ASN][1000 genomes] |
rs66543122 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs66569903 | 1.00[ASN][1000 genomes] |
rs66574092 | 1.00[ASN][1000 genomes] |
rs66589206 | 1.00[ASN][1000 genomes] |
rs66606466 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs66624731 | 1.00[ASN][1000 genomes] |
rs66629114 | 1.00[ASN][1000 genomes] |
rs66680519 | 1.00[ASN][1000 genomes] |
rs66721237 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs66739429 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs66761801 | 1.00[ASN][1000 genomes] |
rs66796553 | 1.00[ASN][1000 genomes] |
rs66824103 | 1.00[ASN][1000 genomes] |
rs66881017 | 1.00[ASN][1000 genomes] |
rs66920061 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs66935924 | 1.00[ASN][1000 genomes] |
rs66952248 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs66983270 | 1.00[ASN][1000 genomes] |
rs66995551 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs67126124 | 1.00[ASN][1000 genomes] |
rs67136611 | 1.00[ASN][1000 genomes] |
rs67152262 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs67224165 | 1.00[ASN][1000 genomes] |
rs67261476 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs67311221 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs67347619 | 1.00[ASN][1000 genomes] |
rs67399263 | 1.00[ASN][1000 genomes] |
rs67407309 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs67434511 | 0.92[ASN][1000 genomes] |
rs67448624 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs67535999 | 1.00[ASN][1000 genomes] |
rs67562061 | 1.00[ASN][1000 genomes] |
rs67580367 | 1.00[ASN][1000 genomes] |
rs67639118 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs67642342 | 1.00[ASN][1000 genomes] |
rs67654202 | 1.00[ASN][1000 genomes] |
rs67687334 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs67691941 | 1.00[ASN][1000 genomes] |
rs67735893 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs67748606 | 1.00[ASN][1000 genomes] |
rs67751006 | 1.00[ASN][1000 genomes] |
rs67755243 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs67768352 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs67823383 | 1.00[ASN][1000 genomes] |
rs67825879 | 1.00[ASN][1000 genomes] |
rs67840505 | 1.00[ASN][1000 genomes] |
rs67980276 | 1.00[ASN][1000 genomes] |
rs67982985 | 1.00[ASN][1000 genomes] |
rs68008015 | 1.00[ASN][1000 genomes] |
rs68009363 | 1.00[ASN][1000 genomes] |
rs68030146 | 1.00[ASN][1000 genomes] |
rs68133325 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs68145579 | 1.00[ASN][1000 genomes] |
rs68166481 | 1.00[ASN][1000 genomes] |
rs71078956 | 1.00[ASN][1000 genomes] |
rs7305593 | 1.00[ASN][1000 genomes] |
rs73175427 | 1.00[ASN][1000 genomes] |
rs73175468 | 1.00[ASN][1000 genomes] |
rs73175480 | 1.00[ASN][1000 genomes] |
rs73175494 | 1.00[ASN][1000 genomes] |
rs73179849 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs73179855 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs73179857 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs73181416 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs73181428 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs73181432 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs73181435 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs73181441 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs73192720 | 1.00[ASN][1000 genomes] |
rs73192732 | 1.00[ASN][1000 genomes] |
rs73192749 | 1.00[ASN][1000 genomes] |
rs73192760 | 1.00[ASN][1000 genomes] |
rs73393740 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73393778 | 1.00[AMR][1000 genomes] |
rs73400125 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73400158 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73408641 | 1.00[AMR][1000 genomes] |
rs73408682 | 1.00[AMR][1000 genomes] |
rs73410067 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73410102 | 1.00[AMR][1000 genomes] |
rs73412009 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73412012 | 1.00[AMR][1000 genomes] |
rs73412014 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73412072 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73412073 | 1.00[AMR][1000 genomes] |
rs73412076 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73412087 | 1.00[AMR][1000 genomes] |
rs73412095 | 1.00[AMR][1000 genomes] |
rs73414089 | 1.00[AMR][1000 genomes] |
rs73414095 | 1.00[AMR][1000 genomes] |
rs73414099 | 1.00[AMR][1000 genomes] |
rs73414185 | 1.00[AMR][1000 genomes] |
rs73416003 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2754127 | chr12:86723232-87576932 | Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv916862 | chr12:86837694-87718558 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv899397 | chr12:86863041-87636831 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
4 | nsv868879 | chr12:87207243-87578373 | Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
5 | nsv559693 | chr12:87216285-87447757 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
6 | nsv1052693 | chr12:87219949-87573582 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
7 | nsv899403 | chr12:87225050-87528020 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
8 | esv2753551 | chr12:87226774-87473947 | Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Weak transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
9 | nsv899406 | chr12:87233995-87528020 | Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
10 | nsv899407 | chr12:87254691-87506910 | Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
11 | esv2752961 | chr12:87255339-87465826 | ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Active TSS Weak transcription | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
12 | esv2754599 | chr12:87255339-87491053 | Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
13 | esv2755612 | chr12:87260646-87460465 | Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
14 | esv2755080 | chr12:87260646-87465826 | Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
15 | esv2754967 | chr12:87281456-87491053 | ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
16 | nsv519543 | chr12:87307329-87528020 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
17 | nsv899408 | chr12:87319908-87490752 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
18 | nsv899409 | chr12:87319908-87506910 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
19 | nsv899410 | chr12:87319908-87528020 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
20 | nsv899411 | chr12:87339195-87459912 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
21 | nsv899412 | chr12:87346094-87506910 | Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
22 | nsv899413 | chr12:87378980-87490752 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
23 | nsv899414 | chr12:87378980-87506910 | Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
24 | nsv559698 | chr12:87435308-87479405 | Enhancers ZNF genes & repeats Weak transcription | n/a | n/a | inside rSNPs | diseases |
25 | esv3360874 | chr12:87441921-87445819 | Enhancers Weak transcription | n/a | n/a | inside rSNPs | diseases |
26 | nsv559699 | chr12:87442480-87491505 | Weak transcription ZNF genes & repeats Enhancers | n/a | n/a | inside rSNPs | diseases |
27 | nsv899415 | chr12:87442480-87528020 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
28 | nsv899416 | chr12:87442480-87588533 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:87442000-87448400 | Weak transcription | Fetal Brain Male | brain |
2 | chr12:87445000-87445800 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
3 | chr12:87445200-87446200 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
4 | chr12:87445400-87445800 | Enhancers | A549 | lung |