Variant report
Variant | rs2372003 |
---|---|
Chromosome Location | chr2:35747362-35747363 |
allele | A/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] |
---|---|
rs10171178 | 0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs10171609 | 0.85[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs10175485 | 0.81[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs10179444 | 0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs10190386 | 0.84[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs10195463 | 0.91[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs10198577 | 1.00[ASN][1000 genomes] |
rs10207695 | 0.89[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs10495842 | 0.87[AMR][1000 genomes] |
rs11681520 | 0.87[AFR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs11682305 | 0.83[AFR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs11687904 | 0.88[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs12712442 | 0.87[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs12712443 | 0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs12712444 | 0.82[AFR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs12712447 | 1.00[ASN][1000 genomes] |
rs12712461 | 0.87[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs13007143 | 0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs13023651 | 0.85[AFR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs13024477 | 0.87[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs13384218 | 1.00[ASN][1000 genomes] |
rs13401687 | 0.82[ASN][1000 genomes] |
rs13403661 | 0.92[ASN][1000 genomes] |
rs13421752 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1347941 | 0.87[AMR][1000 genomes] |
rs1439709 | 0.91[ASN][1000 genomes] |
rs1439715 | 0.89[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs1898940 | 0.87[AMR][1000 genomes] |
rs1960283 | 1.00[ASN][1000 genomes] |
rs2372009 | 0.89[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs34925908 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35093970 | 0.90[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs35339230 | 0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs35404436 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35482291 | 0.90[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs35855779 | 0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs35940299 | 0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs36063839 | 0.90[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs36108127 | 1.00[ASN][1000 genomes] |
rs6543946 | 0.81[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs6543947 | 0.85[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs6543948 | 0.90[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6543952 | 0.94[ASN][1000 genomes] |
rs6543953 | 0.85[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6543955 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs66494409 | 0.85[AMR][1000 genomes] |
rs6713339 | 0.90[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6720204 | 0.88[AMR][1000 genomes] |
rs6734971 | 0.89[AMR][1000 genomes] |
rs6737642 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6739508 | 0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs71451224 | 0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs71451225 | 0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs71451226 | 0.86[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7557364 | 0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7557690 | 0.86[ASN][1000 genomes] |
rs7561183 | 0.91[ASN][1000 genomes] |
rs7579592 | 0.94[ASN][1000 genomes] |
rs7579668 | 0.89[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs7597745 | 0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7597849 | 0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7606170 | 0.91[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7606290 | 0.90[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7606733 | 0.87[AMR][1000 genomes] |
rs9308968 | 0.86[ASN][1000 genomes] |
rs9308969 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9749688 | 0.82[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1010722 | chr2:35072575-35950219 | Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 8 gene(s) | inside rSNPs | diseases |
2 | nsv519522 | chr2:35425529-35861883 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv1008651 | chr2:35469467-35896486 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv999139 | chr2:35483033-35860024 | Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 3 gene(s) | inside rSNPs | diseases |
5 | nsv535636 | chr2:35483033-35860024 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 3 gene(s) | inside rSNPs | diseases |
6 | nsv873848 | chr2:35641532-35973963 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Strong transcription | TF binding regionChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
7 | nsv949472 | chr2:35709203-36447481 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
8 | nsv518450 | chr2:35711861-35779358 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
9 | nsv1009123 | chr2:35728920-36412880 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
10 | nsv535639 | chr2:35728920-36412880 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
11 | nsv998313 | chr2:35731937-36422991 | ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
12 | nsv535640 | chr2:35731937-36422991 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:35743800-35747600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr2:35743800-35754600 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
3 | chr2:35747000-35748000 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
4 | chr2:35747000-35748200 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
5 | chr2:35747000-35748200 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
6 | chr2:35747200-35747800 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
7 | chr2:35747200-35748000 | Enhancers | iPS DF 6.9 Cell Line | embryonic stem cell |