Variant report
Variant | rs35986835 |
---|---|
Chromosome Location | chr13:39417065-39417066 |
allele | G/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] |
---|---|
rs11618742 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs12864816 | 1.00[ASN][1000 genomes] |
rs12869426 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs12869876 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs12869917 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs12875224 | 1.00[ASN][1000 genomes] |
rs1333506 | 1.00[ASN][1000 genomes] |
rs1333508 | 1.00[ASN][1000 genomes] |
rs1945496 | 1.00[ASN][1000 genomes] |
rs34127262 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35252750 | 1.00[ASN][1000 genomes] |
rs35429023 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs35459396 | 1.00[ASN][1000 genomes] |
rs35657252 | 1.00[ASN][1000 genomes] |
rs35944548 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs36088006 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs4287442 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs4334155 | 1.00[ASN][1000 genomes] |
rs4369521 | 1.00[ASN][1000 genomes] |
rs4397983 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs4426230 | 1.00[ASN][1000 genomes] |
rs4426231 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs4533148 | 1.00[ASN][1000 genomes] |
rs4643179 | 1.00[ASN][1000 genomes] |
rs4943606 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4943607 | 1.00[ASN][1000 genomes] |
rs4943608 | 1.00[ASN][1000 genomes] |
rs4943609 | 1.00[ASN][1000 genomes] |
rs4943610 | 1.00[ASN][1000 genomes] |
rs4943611 | 1.00[ASN][1000 genomes] |
rs4943612 | 1.00[ASN][1000 genomes] |
rs4943615 | 1.00[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs61945515 | 1.00[ASN][1000 genomes] |
rs61945516 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs61947983 | 1.00[ASN][1000 genomes] |
rs61948017 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs61948018 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs66889481 | 1.00[ASN][1000 genomes] |
rs71198492 | 1.00[ASN][1000 genomes] |
rs71423186 | 1.00[ASN][1000 genomes] |
rs71423187 | 1.00[ASN][1000 genomes] |
rs71439788 | 1.00[ASN][1000 genomes] |
rs71439789 | 1.00[ASN][1000 genomes] |
rs7328953 | 1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs7331927 | 1.00[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs7982313 | 1.00[ASN][1000 genomes] |
rs9532285 | 1.00[ASN][1000 genomes] |
rs9532287 | 1.00[ASN][1000 genomes] |
rs9532288 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9532294 | 1.00[ASN][1000 genomes] |
rs9532297 | 1.00[ASN][1000 genomes] |
rs9532298 | 1.00[ASN][1000 genomes] |
rs9532310 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs9548466 | 0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9548467 | 1.00[ASN][1000 genomes] |
rs9548468 | 1.00[ASN][1000 genomes] |
rs9548471 | 1.00[ASN][1000 genomes] |
rs9548473 | 1.00[ASN][1000 genomes] |
rs9548474 | 1.00[ASN][1000 genomes] |
rs9548475 | 1.00[ASN][1000 genomes] |
rs9548476 | 1.00[ASN][1000 genomes] |
rs9548478 | 1.00[ASN][1000 genomes] |
rs9548479 | 1.00[ASN][1000 genomes] |
rs9548480 | 1.00[ASN][1000 genomes] |
rs9548488 | 1.00[ASN][1000 genomes] |
rs9548489 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9548490 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9548492 | 1.00[ASN][1000 genomes] |
rs9548493 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9548494 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9548495 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9548496 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9548497 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9548498 | 1.00[ASN][1000 genomes] |
rs9548499 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9548500 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9548501 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9548502 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9548503 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9548504 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9548505 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9548507 | 1.00[ASN][1000 genomes] |
rs9548515 | 1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9548521 | 1.00[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs9548523 | 1.00[ASN][1000 genomes] |
rs9548524 | 1.00[ASN][1000 genomes] |
rs9548525 | 1.00[ASN][1000 genomes] |
rs9548531 | 1.00[ASN][1000 genomes] |
rs9548532 | 1.00[ASN][1000 genomes] |
rs9548535 | 1.00[ASN][1000 genomes] |
rs9548552 | 1.00[ASN][1000 genomes] |
rs9548554 | 1.00[ASN][1000 genomes] |
rs9548555 | 1.00[ASN][1000 genomes] |
rs9548556 | 1.00[ASN][1000 genomes] |
rs9548557 | 1.00[ASN][1000 genomes] |
rs9548560 | 1.00[ASN][1000 genomes] |
rs9548562 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs9548563 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs9548569 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs9548573 | 1.00[ASN][1000 genomes] |
rs9548576 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv832585 | chr13:39233307-39424375 | Weak transcription Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
2 | esv2754118 | chr13:39347702-40222644 | Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:39389400-39423000 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
2 | chr13:39394600-39423000 | Weak transcription | Fetal Kidney | kidney |
3 | chr13:39414000-39420800 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
4 | chr13:39414600-39422600 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
5 | chr13:39414600-39425400 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
6 | chr13:39415800-39418600 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
7 | chr13:39416200-39450200 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
8 | chr13:39416800-39417400 | Enhancers | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |