Variant report
Variant | rs73175487 |
---|---|
Chromosome Location | chr12:87402710-87402711 |
allele | C/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[EUR][1000 genomes] |
rs11104222 | 1.00[EUR][1000 genomes] |
rs11104241 | 1.00[EUR][1000 genomes] |
rs11104353 | 0.95[EUR][1000 genomes] |
rs11608450 | 1.00[EUR][1000 genomes] |
rs11608474 | 1.00[EUR][1000 genomes] |
rs11608968 | 1.00[AMR][1000 genomes] |
rs11609545 | 1.00[EUR][1000 genomes] |
rs11609577 | 1.00[EUR][1000 genomes] |
rs11609959 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs11610000 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11610202 | 1.00[EUR][1000 genomes] |
rs11610236 | 1.00[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs11610240 | 1.00[EUR][1000 genomes] |
rs11610610 | 1.00[EUR][1000 genomes] |
rs11611298 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11611539 | 1.00[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs11612996 | 1.00[EUR][1000 genomes] |
rs11613608 | 1.00[EUR][1000 genomes] |
rs11614902 | 1.00[EUR][1000 genomes] |
rs11615280 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11615328 | 1.00[EUR][1000 genomes] |
rs11615381 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12099694 | 1.00[EUR][1000 genomes] |
rs12099773 | 1.00[EUR][1000 genomes] |
rs12099774 | 1.00[EUR][1000 genomes] |
rs12301215 | 1.00[EUR][1000 genomes] |
rs17014343 | 1.00[EUR][1000 genomes] |
rs17014345 | 1.00[EUR][1000 genomes] |
rs17014347 | 1.00[EUR][1000 genomes] |
rs17014352 | 1.00[EUR][1000 genomes] |
rs17014355 | 1.00[EUR][1000 genomes] |
rs17014357 | 1.00[EUR][1000 genomes] |
rs17014359 | 1.00[EUR][1000 genomes] |
rs17014361 | 1.00[EUR][1000 genomes] |
rs17014363 | 1.00[EUR][1000 genomes] |
rs17014366 | 1.00[EUR][1000 genomes] |
rs17014369 | 1.00[EUR][1000 genomes] |
rs17014430 | 1.00[EUR][1000 genomes] |
rs28438801 | 0.89[EUR][1000 genomes] |
rs34212176 | 1.00[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs35772317 | 1.00[EUR][1000 genomes] |
rs55675470 | 1.00[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs55676823 | 1.00[EUR][1000 genomes] |
rs55742281 | 0.89[EUR][1000 genomes] |
rs55768272 | 1.00[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs55778807 | 1.00[EUR][1000 genomes] |
rs55844216 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56212508 | 0.89[EUR][1000 genomes] |
rs56337441 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56350179 | 1.00[EUR][1000 genomes] |
rs59432611 | 0.89[EUR][1000 genomes] |
rs60530487 | 1.00[EUR][1000 genomes] |
rs60718562 | 1.00[EUR][1000 genomes] |
rs61619114 | 0.89[EUR][1000 genomes] |
rs66473769 | 0.89[EUR][1000 genomes] |
rs66489945 | 0.95[EUR][1000 genomes] |
rs66507120 | 1.00[EUR][1000 genomes] |
rs66520580 | 0.95[EUR][1000 genomes] |
rs66543122 | 1.00[EUR][1000 genomes] |
rs66569903 | 1.00[EUR][1000 genomes] |
rs66574092 | 1.00[EUR][1000 genomes] |
rs66589206 | 1.00[EUR][1000 genomes] |
rs66606466 | 1.00[EUR][1000 genomes] |
rs66624731 | 1.00[EUR][1000 genomes] |
rs66629114 | 0.89[EUR][1000 genomes] |
rs66680519 | 0.89[EUR][1000 genomes] |
rs66721237 | 1.00[EUR][1000 genomes] |
rs66739429 | 1.00[EUR][1000 genomes] |
rs66761801 | 1.00[EUR][1000 genomes] |
rs66796553 | 1.00[EUR][1000 genomes] |
rs66824103 | 0.89[EUR][1000 genomes] |
rs66881017 | 1.00[EUR][1000 genomes] |
rs66920061 | 1.00[EUR][1000 genomes] |
rs66935924 | 1.00[EUR][1000 genomes] |
rs66952248 | 1.00[EUR][1000 genomes] |
rs66983270 | 1.00[EUR][1000 genomes] |
rs66995551 | 1.00[EUR][1000 genomes] |
rs67126124 | 1.00[EUR][1000 genomes] |
rs67136611 | 1.00[EUR][1000 genomes] |
rs67152262 | 1.00[EUR][1000 genomes] |
rs67224165 | 0.89[EUR][1000 genomes] |
rs67261476 | 1.00[EUR][1000 genomes] |
rs67311221 | 1.00[EUR][1000 genomes] |
rs67347619 | 0.89[EUR][1000 genomes] |
rs67399263 | 1.00[EUR][1000 genomes] |
rs67407309 | 1.00[EUR][1000 genomes] |
rs67429282 | 1.00[EUR][1000 genomes] |
rs67448624 | 1.00[EUR][1000 genomes] |
rs67535999 | 1.00[EUR][1000 genomes] |
rs67562061 | 1.00[EUR][1000 genomes] |
rs67639118 | 1.00[EUR][1000 genomes] |
rs67642342 | 1.00[EUR][1000 genomes] |
rs67651962 | 0.95[EUR][1000 genomes] |
rs67654202 | 0.89[EUR][1000 genomes] |
rs67687334 | 1.00[EUR][1000 genomes] |
rs67691941 | 1.00[EUR][1000 genomes] |
rs67735893 | 1.00[EUR][1000 genomes] |
rs67748606 | 0.90[EUR][1000 genomes] |
rs67751006 | 1.00[EUR][1000 genomes] |
rs67755243 | 1.00[EUR][1000 genomes] |
rs67768352 | 1.00[EUR][1000 genomes] |
rs67823383 | 1.00[EUR][1000 genomes] |
rs67825879 | 0.89[EUR][1000 genomes] |
rs67840505 | 1.00[EUR][1000 genomes] |
rs67964737 | 0.95[EUR][1000 genomes] |
rs67980276 | 1.00[EUR][1000 genomes] |
rs67982985 | 1.00[EUR][1000 genomes] |
rs68008015 | 1.00[EUR][1000 genomes] |
rs68009363 | 1.00[EUR][1000 genomes] |
rs68030146 | 1.00[EUR][1000 genomes] |
rs68133325 | 1.00[EUR][1000 genomes] |
rs68145579 | 0.90[EUR][1000 genomes] |
rs68166481 | 0.86[EUR][1000 genomes] |
rs71078956 | 1.00[EUR][1000 genomes] |
rs7305593 | 1.00[EUR][1000 genomes] |
rs73175412 | 1.00[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs73175417 | 1.00[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs73175427 | 0.89[EUR][1000 genomes] |
rs73175466 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73175468 | 1.00[EUR][1000 genomes] |
rs73175469 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73175473 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73175476 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73175480 | 1.00[EUR][1000 genomes] |
rs73175482 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73175494 | 1.00[EUR][1000 genomes] |
rs73175495 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73175498 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73175502 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73177627 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73177634 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73177637 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73177701 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73179835 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73179837 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73179847 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73179849 | 1.00[EUR][1000 genomes] |
rs73179855 | 1.00[EUR][1000 genomes] |
rs73179857 | 0.90[EUR][1000 genomes] |
rs73181416 | 1.00[EUR][1000 genomes] |
rs73181421 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73181428 | 1.00[EUR][1000 genomes] |
rs73181432 | 1.00[EUR][1000 genomes] |
rs73181435 | 1.00[EUR][1000 genomes] |
rs73181437 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73181441 | 0.90[EUR][1000 genomes] |
rs73191081 | 1.00[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs73192706 | 1.00[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs73192712 | 1.00[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs73192720 | 0.89[EUR][1000 genomes] |
rs73192732 | 0.89[EUR][1000 genomes] |
rs73192735 | 1.00[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs73192741 | 1.00[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs73192749 | 0.89[EUR][1000 genomes] |
rs73192750 | 1.00[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs73192753 | 1.00[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs73192760 | 0.89[EUR][1000 genomes] |
rs73192766 | 1.00[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs73194307 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs73194312 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs73194315 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs73194345 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs73194353 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs73194356 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs73194359 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs73197878 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73197888 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73197891 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73197895 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73199707 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs73199710 | 1.00[AMR][1000 genomes];0.95[EUR][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 | nsv1049688 | chr12:87219949-87412043 | Enhancers ZNF genes & repeats Active TSS Weak transcription Strong transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
7 | 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 |
8 | 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 |
9 | 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 |
10 | nsv899405 | chr12:87233995-87430209 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
11 | 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 |
12 | nsv428596 | chr12:87244257-87422246 | Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
13 | 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 |
14 | 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 |
15 | 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 |
16 | 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 |
17 | 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 |
18 | 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 |
19 | 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 |
20 | nsv517718 | chr12:87319908-87430209 | Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
21 | 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 |
22 | 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 |
23 | 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 |
24 | nsv1048789 | chr12:87321296-87413371 | Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
25 | 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 |
26 | 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 |
27 | nsv1044248 | chr12:87357657-87444309 | Weak transcription ZNF genes & repeats Active TSS Strong transcription Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
28 | nsv1043132 | chr12:87363498-87428530 | Enhancers ZNF genes & repeats Active TSS Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
29 | nsv1044646 | chr12:87369654-87426259 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
30 | nsv1049612 | chr12:87369654-87430209 | Weak transcription ZNF genes & repeats Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
31 | nsv1053777 | chr12:87369654-87432340 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
32 | nsv1052738 | chr12:87369654-87440463 | Weak transcription ZNF genes & repeats Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
33 | nsv899413 | chr12:87378980-87490752 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
34 | nsv899414 | chr12:87378980-87506910 | Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
35 | nsv806 | chr12:87382310-87427506 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:87398800-87424000 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
2 | chr12:87402400-87403000 | Enhancers | Liver | Liver |