Variant report
Variant | rs73479276 |
---|---|
Chromosome Location | chr6:63065737-63065738 |
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] |
---|---|
rs1041667 | 0.82[ASN][1000 genomes] |
rs1317933 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs16880659 | 0.82[ASN][1000 genomes] |
rs16881826 | 0.82[ASN][1000 genomes] |
rs16882220 | 0.82[ASN][1000 genomes] |
rs16882668 | 0.82[ASN][1000 genomes] |
rs16882700 | 0.82[ASN][1000 genomes] |
rs16882802 | 0.82[ASN][1000 genomes] |
rs16882808 | 0.82[ASN][1000 genomes] |
rs35018276 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs59606233 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs62414735 | 0.82[ASN][1000 genomes] |
rs62414736 | 0.82[ASN][1000 genomes] |
rs62414740 | 0.82[ASN][1000 genomes] |
rs62414741 | 0.82[ASN][1000 genomes] |
rs62414745 | 0.82[ASN][1000 genomes] |
rs62414746 | 0.82[ASN][1000 genomes] |
rs62414747 | 0.82[ASN][1000 genomes] |
rs62416846 | 0.82[ASN][1000 genomes] |
rs62416847 | 0.82[ASN][1000 genomes] |
rs62416848 | 0.82[ASN][1000 genomes] |
rs62416859 | 0.82[ASN][1000 genomes] |
rs62418175 | 0.82[ASN][1000 genomes] |
rs62418203 | 0.82[ASN][1000 genomes] |
rs62418213 | 0.82[ASN][1000 genomes] |
rs62418216 | 0.82[ASN][1000 genomes] |
rs62418218 | 0.82[ASN][1000 genomes] |
rs6453554 | 0.82[ASN][1000 genomes] |
rs6453555 | 0.82[ASN][1000 genomes] |
rs6918824 | 0.82[ASN][1000 genomes] |
rs6930175 | 0.82[ASN][1000 genomes] |
rs6931088 | 0.82[ASN][1000 genomes] |
rs6937433 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73479292 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73479294 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73479298 | 1.00[AMR][1000 genomes] |
rs73484928 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs7751345 | 0.82[ASN][1000 genomes] |
rs7754074 | 0.82[ASN][1000 genomes] |
rs7756645 | 0.82[ASN][1000 genomes] |
rs876855 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1017249 | chr6:62906813-63317382 | Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv1020677 | chr6:62911584-63309663 | Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv532025 | chr6:62944349-63571677 | Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
4 | nsv916760 | chr6:62944661-63290986 | Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
5 | nsv1029503 | chr6:63033365-63698355 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:63064800-63067600 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |