Variant report
Variant | rs73090942 |
---|---|
Chromosome Location | chr1:227721333-227721334 |
allele | A/G |
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)
No data |
No data |
(count:2 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs12089076 | 1.00[AMR][1000 genomes] |
rs12563564 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs12564917 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs12565618 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs12565653 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs12567084 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16847822 | 1.00[AMR][1000 genomes] |
rs16847912 | 1.00[AMR][1000 genomes] |
rs16847929 | 1.00[AMR][1000 genomes] |
rs16847987 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16859962 | 1.00[AMR][1000 genomes] |
rs16860227 | 1.00[AMR][1000 genomes] |
rs17492447 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs2101862 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs2313220 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs35703429 | 1.00[AMR][1000 genomes] |
rs57165550 | 1.00[AMR][1000 genomes] |
rs58322371 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs59404931 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs59461077 | 1.00[AMR][1000 genomes] |
rs59772630 | 1.00[AMR][1000 genomes] |
rs60835672 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs61283390 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs6665512 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs6675470 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73088936 | 1.00[AMR][1000 genomes] |
rs73090912 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73090935 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73090936 | 1.00[AMR][1000 genomes] |
rs73090937 | 1.00[AMR][1000 genomes] |
rs73090938 | 1.00[AMR][1000 genomes] |
rs73090947 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73090948 | 1.00[AMR][1000 genomes] |
rs73090952 | 1.00[AMR][1000 genomes] |
rs73090959 | 1.00[AMR][1000 genomes] |
rs73090985 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73090986 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73090987 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73090994 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73090995 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73091000 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73092604 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73092607 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73092610 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73092646 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73092653 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73092661 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73092665 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73093304 | 1.00[AMR][1000 genomes] |
rs73093319 | 1.00[AMR][1000 genomes] |
rs73094528 | 1.00[AMR][1000 genomes] |
rs73094536 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73094538 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73094556 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73094558 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73094561 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73094566 | 0.82[AFR][1000 genomes] |
rs73094571 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73099300 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73099302 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73101625 | 1.00[AMR][1000 genomes] |
rs73101653 | 1.00[AMR][1000 genomes] |
rs73102372 | 1.00[AMR][1000 genomes] |
rs73102384 | 1.00[AMR][1000 genomes] |
rs73102391 | 1.00[AMR][1000 genomes] |
rs73104364 | 1.00[AMR][1000 genomes] |
rs7526436 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7546845 | 1.00[AMR][1000 genomes] |
rs7554851 | 1.00[AMR][1000 genomes] |
rs7554870 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv534002 | chr1:227315186-228047108 | Bivalent/Poised TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 54 gene(s) | inside rSNPs | diseases |
2 | esv2753828 | chr1:227670265-227791265 | Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
3 | nsv873244 | chr1:227682414-227736363 | Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
4 | nsv873246 | chr1:227694948-227884465 | Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
5 | nsv1007479 | chr1:227695868-227984466 | Genic enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 33 gene(s) | inside rSNPs | diseases |
6 | nsv873247 | chr1:227697381-227736363 | Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
7 | nsv873248 | chr1:227710381-227786033 | ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 6 gene(s) | inside rSNPs | diseases |
8 | nsv945338 | chr1:227712483-227722545 | ZNF genes & repeats Weak transcription Enhancers | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:227714200-227721800 | ZNF genes & repeats | Liver | Liver |
2 | chr1:227715600-227721600 | ZNF genes & repeats | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
3 | chr1:227718600-227723200 | Weak transcription | Psoas Muscle | Psoas |
4 | chr1:227720000-227722000 | ZNF genes & repeats | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
5 | chr1:227720800-227725800 | Weak transcription | Pancreas | Pancrea |
6 | chr1:227720800-227729200 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
7 | chr1:227720800-227729200 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
8 | chr1:227721200-227725800 | Weak transcription | Aorta | Aorta |