Variant report
Variant | rs28588337 |
---|---|
Chromosome Location | chr3:191330044-191330045 |
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] |
---|---|
rs10937504 | 0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11715205 | 0.81[EUR][1000 genomes] |
rs11918752 | 1.00[ASN][1000 genomes] |
rs11919586 | 1.00[ASN][1000 genomes] |
rs11922711 | 1.00[ASN][1000 genomes] |
rs11923709 | 1.00[ASN][1000 genomes] |
rs11923905 | 1.00[ASN][1000 genomes] |
rs11924646 | 1.00[ASN][1000 genomes] |
rs11924686 | 1.00[ASN][1000 genomes] |
rs11927215 | 1.00[ASN][1000 genomes] |
rs13060140 | 1.00[ASN][1000 genomes] |
rs13061247 | 1.00[ASN][1000 genomes] |
rs13061286 | 1.00[ASN][1000 genomes] |
rs13061344 | 1.00[ASN][1000 genomes] |
rs13061416 | 1.00[ASN][1000 genomes] |
rs13061555 | 0.88[EUR][1000 genomes] |
rs13062368 | 1.00[ASN][1000 genomes] |
rs13062859 | 1.00[ASN][1000 genomes] |
rs13063760 | 1.00[ASN][1000 genomes] |
rs13065834 | 1.00[ASN][1000 genomes] |
rs13067446 | 1.00[ASN][1000 genomes] |
rs13068594 | 1.00[ASN][1000 genomes] |
rs13068608 | 1.00[ASN][1000 genomes] |
rs13073576 | 1.00[ASN][1000 genomes] |
rs13074553 | 1.00[ASN][1000 genomes] |
rs13074573 | 1.00[ASN][1000 genomes] |
rs13074735 | 1.00[ASN][1000 genomes] |
rs13074869 | 1.00[ASN][1000 genomes] |
rs13075002 | 1.00[ASN][1000 genomes] |
rs13075042 | 1.00[ASN][1000 genomes] |
rs13075337 | 1.00[ASN][1000 genomes] |
rs13075638 | 1.00[ASN][1000 genomes] |
rs13075894 | 1.00[ASN][1000 genomes] |
rs13079207 | 1.00[ASN][1000 genomes] |
rs13079761 | 1.00[ASN][1000 genomes] |
rs13079895 | 1.00[ASN][1000 genomes] |
rs13081466 | 0.86[ASN][1000 genomes] |
rs13083205 | 1.00[ASN][1000 genomes] |
rs13083390 | 1.00[ASN][1000 genomes] |
rs13085670 | 1.00[ASN][1000 genomes] |
rs13086688 | 1.00[ASN][1000 genomes] |
rs13088741 | 1.00[ASN][1000 genomes] |
rs13089478 | 1.00[ASN][1000 genomes] |
rs13089779 | 0.88[EUR][1000 genomes] |
rs13090447 | 1.00[ASN][1000 genomes] |
rs13091849 | 1.00[ASN][1000 genomes] |
rs13091896 | 1.00[ASN][1000 genomes] |
rs13092013 | 1.00[ASN][1000 genomes] |
rs13092899 | 1.00[ASN][1000 genomes] |
rs13093608 | 1.00[ASN][1000 genomes] |
rs13097345 | 1.00[ASN][1000 genomes] |
rs13099777 | 1.00[ASN][1000 genomes] |
rs13099909 | 1.00[ASN][1000 genomes] |
rs13099935 | 1.00[ASN][1000 genomes] |
rs13100016 | 1.00[ASN][1000 genomes] |
rs13100217 | 1.00[ASN][1000 genomes] |
rs13100368 | 1.00[ASN][1000 genomes] |
rs13100538 | 1.00[ASN][1000 genomes] |
rs1806334 | 1.00[ASN][1000 genomes] |
rs1806335 | 1.00[ASN][1000 genomes] |
rs1851684 | 0.86[EUR][1000 genomes] |
rs1916631 | 1.00[ASN][1000 genomes] |
rs1916632 | 1.00[ASN][1000 genomes] |
rs1916637 | 0.87[EUR][1000 genomes] |
rs34175932 | 1.00[ASN][1000 genomes] |
rs34180265 | 0.85[EUR][1000 genomes] |
rs34182626 | 1.00[ASN][1000 genomes] |
rs34372317 | 1.00[ASN][1000 genomes] |
rs34417776 | 1.00[ASN][1000 genomes] |
rs34541697 | 1.00[ASN][1000 genomes] |
rs34756413 | 1.00[ASN][1000 genomes] |
rs34758139 | 1.00[ASN][1000 genomes] |
rs34882440 | 1.00[ASN][1000 genomes] |
rs34938847 | 1.00[ASN][1000 genomes] |
rs35102890 | 1.00[ASN][1000 genomes] |
rs35171857 | 1.00[ASN][1000 genomes] |
rs35295700 | 1.00[ASN][1000 genomes] |
rs35311163 | 1.00[ASN][1000 genomes] |
rs35322276 | 1.00[ASN][1000 genomes] |
rs35443405 | 1.00[ASN][1000 genomes] |
rs35486591 | 1.00[ASN][1000 genomes] |
rs35645410 | 1.00[ASN][1000 genomes] |
rs35689458 | 1.00[ASN][1000 genomes] |
rs35794875 | 1.00[ASN][1000 genomes] |
rs35826551 | 1.00[ASN][1000 genomes] |
rs35906203 | 1.00[ASN][1000 genomes] |
rs36021699 | 1.00[ASN][1000 genomes] |
rs36036283 | 1.00[ASN][1000 genomes] |
rs36053678 | 1.00[ASN][1000 genomes] |
rs36055292 | 1.00[ASN][1000 genomes] |
rs36074577 | 1.00[ASN][1000 genomes] |
rs36122341 | 1.00[ASN][1000 genomes] |
rs3885870 | 1.00[ASN][1000 genomes] |
rs4282107 | 1.00[ASN][1000 genomes] |
rs4686585 | 0.87[EUR][1000 genomes] |
rs4687246 | 0.84[EUR][1000 genomes] |
rs6768840 | 0.88[EUR][1000 genomes] |
rs6777621 | 0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6785723 | 1.00[ASN][1000 genomes] |
rs71312432 | 1.00[ASN][1000 genomes] |
rs71312434 | 1.00[ASN][1000 genomes] |
rs71312437 | 1.00[ASN][1000 genomes] |
rs71312438 | 1.00[ASN][1000 genomes] |
rs71312440 | 1.00[ASN][1000 genomes] |
rs71635004 | 1.00[ASN][1000 genomes] |
rs7651123 | 0.88[EUR][1000 genomes] |
rs9840419 | 0.82[EUR][1000 genomes] |
rs9847678 | 0.85[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1008969 | chr3:191192569-191383856 | Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh | TF binding regionChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | nsv915689 | chr3:191244719-191479974 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers | TF binding regionChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
3 | nsv997817 | chr3:191284834-191475809 | Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
4 | nsv1001082 | chr3:191320636-191579587 | Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:191325200-191332400 | Weak transcription | HUES6 Cell Line | embryonic stem cell |