Variant report
Variant | rs12749057 |
---|---|
Chromosome Location | chr1:76859040-76859041 |
allele | C/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] |
---|---|
rs1016715 | 0.95[ASN][1000 genomes] |
rs10747346 | 0.95[ASN][1000 genomes] |
rs10747347 | 0.95[ASN][1000 genomes] |
rs10782617 | 0.92[ASN][1000 genomes] |
rs10782619 | 0.95[ASN][1000 genomes] |
rs10873881 | 0.93[ASN][1000 genomes] |
rs10873883 | 0.88[ASN][1000 genomes] |
rs11162135 | 0.95[ASN][1000 genomes] |
rs11162136 | 0.95[ASN][1000 genomes] |
rs11162137 | 0.93[ASN][1000 genomes] |
rs11162138 | 0.86[ASN][1000 genomes] |
rs11162139 | 0.87[ASN][1000 genomes] |
rs11162141 | 0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11162142 | 0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs11162144 | 0.93[ASN][1000 genomes] |
rs11162145 | 0.94[ASN][1000 genomes] |
rs11162146 | 0.94[ASN][1000 genomes] |
rs12021906 | 0.96[ASN][1000 genomes] |
rs12029184 | 0.96[ASN][1000 genomes] |
rs12032409 | 0.87[ASN][1000 genomes] |
rs12034783 | 0.87[ASN][1000 genomes] |
rs12035993 | 0.90[ASN][1000 genomes] |
rs12037958 | 0.94[ASN][1000 genomes] |
rs12038570 | 0.86[ASN][1000 genomes] |
rs12040892 | 0.86[ASN][1000 genomes] |
rs12043272 | 0.94[ASN][1000 genomes] |
rs12046895 | 0.94[ASN][1000 genomes] |
rs12562224 | 0.87[ASN][1000 genomes] |
rs12562911 | 0.84[ASN][1000 genomes] |
rs1325291 | 0.96[ASN][1000 genomes] |
rs1325292 | 0.96[ASN][1000 genomes] |
rs1359467 | 0.91[ASN][1000 genomes] |
rs1359471 | 0.92[ASN][1000 genomes] |
rs1408866 | 0.96[ASN][1000 genomes] |
rs2031482 | 0.96[ASN][1000 genomes] |
rs2147792 | 0.88[ASN][1000 genomes] |
rs4426021 | 0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs4459158 | 0.91[ASN][1000 genomes] |
rs4576696 | 0.91[ASN][1000 genomes] |
rs61771501 | 0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs6664863 | 0.86[ASN][1000 genomes] |
rs6666049 | 0.92[ASN][1000 genomes] |
rs6677296 | 0.94[ASN][1000 genomes] |
rs6678598 | 0.91[ASN][1000 genomes] |
rs67776937 | 0.87[ASN][1000 genomes] |
rs7339997 | 0.93[ASN][1000 genomes] |
rs7340082 | 0.95[ASN][1000 genomes] |
rs9437437 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv870621 | chr1:76620313-76997071 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | nsv534168 | chr1:76718950-77039352 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv1006776 | chr1:76777323-76899975 | Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | nsv1014231 | chr1:76781140-76880630 | Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | nsv462006 | chr1:76826279-77042405 | Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
6 | nsv546585 | chr1:76826279-77042405 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:76858000-76861000 | Weak transcription | Fetal Brain Male | brain |
2 | chr1:76859000-76860000 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |