Variant report
Variant | rs6945733 |
---|---|
Chromosome Location | chr7:119458141-119458142 |
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] |
---|---|
rs10085666 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10233853 | 1.00[EUR][1000 genomes] |
rs10235983 | 1.00[EUR][1000 genomes] |
rs10244657 | 1.00[EUR][1000 genomes] |
rs10247975 | 1.00[EUR][1000 genomes] |
rs10267001 | 0.92[EUR][1000 genomes] |
rs10268381 | 1.00[EUR][1000 genomes] |
rs10274212 | 1.00[EUR][1000 genomes] |
rs10274517 | 1.00[EUR][1000 genomes] |
rs10275081 | 1.00[EUR][1000 genomes] |
rs10281584 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1099822 | 1.00[EUR][1000 genomes] |
rs12333906 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12374758 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12533333 | 1.00[ASN][1000 genomes] |
rs13230241 | 1.00[EUR][1000 genomes] |
rs1357675 | 0.90[EUR][1000 genomes] |
rs1404081 | 1.00[EUR][1000 genomes] |
rs1404082 | 1.00[EUR][1000 genomes] |
rs1404084 | 1.00[EUR][1000 genomes] |
rs1524200 | 1.00[EUR][1000 genomes] |
rs1524201 | 1.00[EUR][1000 genomes] |
rs1524204 | 1.00[EUR][1000 genomes] |
rs1533983 | 1.00[ASN][1000 genomes] |
rs1581503 | 0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1581505 | 1.00[EUR][1000 genomes] |
rs1581506 | 1.00[EUR][1000 genomes] |
rs1589753 | 1.00[EUR][1000 genomes] |
rs1608584 | 1.00[EUR][1000 genomes] |
rs17142322 | 1.00[ASN][1000 genomes] |
rs17142348 | 1.00[ASN][1000 genomes] |
rs17142414 | 1.00[ASN][1000 genomes] |
rs1851807 | 1.00[EUR][1000 genomes] |
rs1916858 | 1.00[ASN][1000 genomes] |
rs1949782 | 1.00[EUR][1000 genomes] |
rs1980321 | 1.00[EUR][1000 genomes] |
rs2049378 | 0.93[EUR][1000 genomes] |
rs2049380 | 1.00[EUR][1000 genomes] |
rs2049382 | 1.00[EUR][1000 genomes] |
rs2049383 | 1.00[EUR][1000 genomes] |
rs2056583 | 1.00[EUR][1000 genomes] |
rs2140567 | 1.00[ASN][1000 genomes] |
rs2140568 | 1.00[ASN][1000 genomes] |
rs2204310 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2204311 | 1.00[EUR][1000 genomes] |
rs2263403 | 1.00[EUR][1000 genomes] |
rs2402487 | 1.00[ASN][1000 genomes] |
rs2402489 | 1.00[EUR][1000 genomes] |
rs28451901 | 1.00[EUR][1000 genomes] |
rs28760947 | 1.00[ASN][1000 genomes] |
rs28776558 | 1.00[ASN][1000 genomes] |
rs4278103 | 1.00[EUR][1000 genomes] |
rs4338035 | 0.90[EUR][1000 genomes] |
rs4449718 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4460311 | 1.00[EUR][1000 genomes] |
rs4493836 | 1.00[ASN][1000 genomes] |
rs4529399 | 0.92[EUR][1000 genomes] |
rs4610676 | 1.00[ASN][1000 genomes] |
rs4727900 | 1.00[EUR][1000 genomes] |
rs4727902 | 1.00[EUR][1000 genomes] |
rs4730942 | 0.90[EUR][1000 genomes] |
rs56291644 | 1.00[ASN][1000 genomes] |
rs58135787 | 1.00[EUR][1000 genomes] |
rs58473239 | 1.00[ASN][1000 genomes] |
rs58538319 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs58859180 | 1.00[EUR][1000 genomes] |
rs60495904 | 1.00[ASN][1000 genomes] |
rs60744696 | 1.00[ASN][1000 genomes] |
rs61081273 | 1.00[ASN][1000 genomes] |
rs6466712 | 1.00[EUR][1000 genomes] |
rs6944434 | 1.00[ASN][1000 genomes] |
rs6947563 | 1.00[ASN][1000 genomes] |
rs6952445 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6954234 | 1.00[ASN][1000 genomes] |
rs6958697 | 0.89[EUR][1000 genomes] |
rs6964883 | 1.00[ASN][1000 genomes] |
rs6964884 | 1.00[ASN][1000 genomes] |
rs6968560 | 1.00[EUR][1000 genomes] |
rs6975903 | 1.00[ASN][1000 genomes] |
rs73472908 | 1.00[ASN][1000 genomes] |
rs73472910 | 1.00[ASN][1000 genomes] |
rs73472916 | 1.00[EUR][1000 genomes] |
rs73472917 | 1.00[EUR][1000 genomes] |
rs73485200 | 1.00[ASN][1000 genomes] |
rs73487136 | 1.00[ASN][1000 genomes] |
rs73487146 | 1.00[ASN][1000 genomes] |
rs73487152 | 1.00[ASN][1000 genomes] |
rs73487156 | 1.00[ASN][1000 genomes] |
rs73487167 | 1.00[ASN][1000 genomes] |
rs73487175 | 1.00[ASN][1000 genomes] |
rs73487178 | 1.00[ASN][1000 genomes] |
rs73487179 | 1.00[ASN][1000 genomes] |
rs73487183 | 1.00[ASN][1000 genomes] |
rs73487186 | 1.00[ASN][1000 genomes] |
rs73487191 | 1.00[ASN][1000 genomes] |
rs73487193 | 1.00[ASN][1000 genomes] |
rs73487195 | 1.00[ASN][1000 genomes] |
rs73487201 | 1.00[ASN][1000 genomes] |
rs73489103 | 1.00[ASN][1000 genomes] |
rs73489107 | 1.00[ASN][1000 genomes] |
rs73489110 | 1.00[ASN][1000 genomes] |
rs73489120 | 1.00[ASN][1000 genomes] |
rs73489137 | 1.00[ASN][1000 genomes] |
rs73489138 | 1.00[ASN][1000 genomes] |
rs73489140 | 1.00[ASN][1000 genomes] |
rs73489143 | 1.00[ASN][1000 genomes] |
rs73489150 | 1.00[ASN][1000 genomes] |
rs73489153 | 1.00[ASN][1000 genomes] |
rs73722666 | 1.00[ASN][1000 genomes] |
rs7779237 | 1.00[EUR][1000 genomes] |
rs7780733 | 1.00[ASN][1000 genomes] |
rs7781144 | 1.00[EUR][1000 genomes] |
rs7782751 | 1.00[EUR][1000 genomes] |
rs7788783 | 1.00[EUR][1000 genomes] |
rs7791400 | 1.00[EUR][1000 genomes] |
rs7797664 | 1.00[ASN][1000 genomes] |
rs7799121 | 1.00[EUR][1000 genomes] |
rs7799517 | 1.00[ASN][1000 genomes] |
rs7808015 | 1.00[EUR][1000 genomes] |
rs7809848 | 1.00[ASN][1000 genomes] |
rs846422 | 1.00[EUR][1000 genomes] |
rs846423 | 1.00[EUR][1000 genomes] |
rs846425 | 1.00[EUR][1000 genomes] |
rs846426 | 1.00[EUR][1000 genomes] |
rs846432 | 1.00[EUR][1000 genomes] |
rs846433 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs846434 | 1.00[EUR][1000 genomes] |
rs846435 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs846440 | 1.00[EUR][1000 genomes] |
rs846442 | 1.00[EUR][1000 genomes] |
rs846443 | 1.00[EUR][1000 genomes] |
rs846449 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs882837 | 1.00[ASN][1000 genomes] |
rs884489 | 1.00[ASN][1000 genomes] |
rs9641626 | 1.00[EUR][1000 genomes] |
rs9641627 | 0.96[EUR][1000 genomes] |
rs9641628 | 1.00[EUR][1000 genomes] |
rs9690438 | 1.00[ASN][1000 genomes] |
rs9691446 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv889115 | chr7:119270386-119577292 | ZNF genes & repeats Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv1029023 | chr7:119292763-119606632 | Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv1023813 | chr7:119292763-119606803 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
4 | nsv524225 | chr7:119293417-119606632 | Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
5 | nsv1029841 | chr7:119299627-119606632 | Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
6 | nsv1024175 | chr7:119299627-119606803 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
7 | nsv1018500 | chr7:119310497-119532489 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS | Chromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
8 | nsv1028812 | chr7:119310497-119604904 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
9 | nsv539097 | chr7:119310497-119604904 | Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
10 | nsv1033418 | chr7:119324894-119600025 | Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
11 | nsv539098 | chr7:119324894-119600025 | Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
12 | nsv608322 | chr7:119363703-119467040 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS | Chromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
13 | nsv608323 | chr7:119363703-119469204 | Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
14 | nsv1018731 | chr7:119411352-119493951 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
15 | nsv1025273 | chr7:119412165-119493951 | Strong transcription Genic enhancers Weak transcription Enhancers Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:119452000-119466600 | Weak transcription | K562 | blood |