Variant report
Variant | rs425232 |
---|---|
Chromosome Location | chr21:47346525-47346526 |
allele | G/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] |
---|---|
rs10854474 | 0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10854475 | 0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11089025 | 1.00[ASN][1000 genomes] |
rs1124309 | 0.83[EUR][1000 genomes] |
rs11701693 | 1.00[ASN][1000 genomes] |
rs1625244 | 0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1736424 | 1.00[ASN][1000 genomes] |
rs1783076 | 1.00[ASN][1000 genomes] |
rs2014421 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs2026286 | 1.00[ASN][1000 genomes] |
rs2150453 | 1.00[CHB][hapmap];0.84[GIH][hapmap];1.00[ASN][1000 genomes] |
rs2150454 | 1.00[ASN][1000 genomes] |
rs2183599 | 0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs2210290 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2277812 | 1.00[ASN][1000 genomes] |
rs2330327 | 0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs2776402 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[EUR][1000 genomes] |
rs2839020 | 0.90[CEU][hapmap];1.00[CHB][hapmap];0.84[GIH][hapmap];0.80[TSI][hapmap];1.00[ASN][1000 genomes] |
rs2839021 | 0.90[CEU][hapmap];1.00[CHB][hapmap];0.89[GIH][hapmap];0.81[TSI][hapmap];1.00[ASN][1000 genomes] |
rs2839030 | 0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs2839033 | 0.90[CEU][hapmap];1.00[CHB][hapmap];0.90[GIH][hapmap];0.84[TSI][hapmap];1.00[ASN][1000 genomes] |
rs2839035 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs2839039 | 0.87[ASW][hapmap];0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.83[LWK][hapmap];0.93[MEX][hapmap];1.00[TSI][hapmap];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2839041 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2839050 | 1.00[ASW][hapmap];0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];0.93[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2839054 | 0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34495634 | 1.00[ASN][1000 genomes] |
rs34686582 | 1.00[CHB][hapmap] |
rs34990419 | 1.00[ASN][1000 genomes] |
rs369245 | 0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs371587 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs373267 | 0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs374331 | 0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs375254 | 0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs375971 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs377213 | 1.00[ASN][1000 genomes] |
rs3788217 | 0.90[CEU][hapmap];1.00[CHB][hapmap];0.90[GIH][hapmap];0.84[TSI][hapmap];1.00[ASN][1000 genomes] |
rs3788218 | 0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs3788226 | 0.90[CEU][hapmap];1.00[CHB][hapmap];0.90[GIH][hapmap];0.84[TSI][hapmap];1.00[ASN][1000 genomes] |
rs3788228 | 0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs379493 | 0.89[EUR][1000 genomes] |
rs379501 | 0.88[EUR][1000 genomes] |
rs380120 | 0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs382195 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs382303 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs402039 | 0.90[CEU][hapmap];1.00[CHB][hapmap];0.85[YRI][hapmap];0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs402355 | 0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs403192 | 0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs407651 | 1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs410902 | 0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs413246 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs413517 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs420386 | 0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs432338 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4369958 | 1.00[ASN][1000 genomes] |
rs439145 | 1.00[ASN][1000 genomes] |
rs442953 | 1.00[ASN][1000 genomes] |
rs451920 | 1.00[ASN][1000 genomes] |
rs452797 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs454268 | 1.00[ASN][1000 genomes] |
rs4818804 | 1.00[ASN][1000 genomes] |
rs4819159 | 0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs56695931 | 1.00[ASN][1000 genomes] |
rs6518257 | 1.00[ASN][1000 genomes] |
rs6518258 | 0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs6518259 | 1.00[ASN][1000 genomes] |
rs71324446 | 1.00[ASN][1000 genomes] |
rs7276114 | 0.90[CEU][hapmap];1.00[CHB][hapmap];0.90[GIH][hapmap];0.84[TSI][hapmap];1.00[ASN][1000 genomes] |
rs7277632 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7279887 | 0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs7280054 | 1.00[ASN][1000 genomes] |
rs7280405 | 0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs7283688 | 1.00[ASN][1000 genomes] |
rs73159604 | 1.00[ASN][1000 genomes] |
rs7410101 | 0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7410105 | 0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs753092 | 0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs760436 | 0.82[CEU][hapmap];0.90[GIH][hapmap] |
rs8131193 | 1.00[CHB][hapmap] |
rs8133932 | 1.00[ASN][1000 genomes] |
rs9637207 | 1.00[ASN][1000 genomes] |
rs9653780 | 0.90[CEU][hapmap];1.00[CHB][hapmap];0.90[GIH][hapmap];0.84[TSI][hapmap];1.00[ASN][1000 genomes] |
rs9653791 | 0.95[CEU][hapmap];1.00[ASN][1000 genomes] |
rs989650 | 1.00[ASN][1000 genomes] |
rs9976042 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv531546 | chr21:46504151-47411772 | Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 93 gene(s) | inside rSNPs | diseases |
2 | nsv1058665 | chr21:46719445-47634282 | Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 91 gene(s) | inside rSNPs | diseases |
3 | nsv544486 | chr21:46719445-47634282 | Bivalent/Poised TSS Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 91 gene(s) | inside rSNPs | diseases |
4 | nsv1059230 | chr21:46956877-47907990 | Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 94 gene(s) | inside rSNPs | n/a |
5 | nsv544491 | chr21:46956877-47907990 | Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 94 gene(s) | inside rSNPs | n/a |
6 | nsv1058472 | chr21:47027823-47797326 | Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 57 gene(s) | inside rSNPs | n/a |
7 | nsv544492 | chr21:47027823-47797326 | Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 57 gene(s) | inside rSNPs | n/a |
8 | nsv428043 | chr21:47179244-47471971 | Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 23 gene(s) | inside rSNPs | n/a |
9 | nsv1065959 | chr21:47188878-48091343 | Bivalent Enhancer Enhancers Genic enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 102 gene(s) | inside rSNPs | n/a |
10 | nsv531580 | chr21:47221774-48090317 | Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 101 gene(s) | inside rSNPs | n/a |
11 | nsv914079 | chr21:47243074-47650362 | Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 35 gene(s) | inside rSNPs | n/a |
12 | nsv914083 | chr21:47265786-47453954 | Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | n/a |
13 | nsv918103 | chr21:47297067-48089510 | Genic enhancers Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 99 gene(s) | inside rSNPs | n/a |
14 | nsv869002 | chr21:47297268-47963186 | Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 73 gene(s) | inside rSNPs | n/a |
15 | nsv1062420 | chr21:47311566-47347666 | Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | n/a |
16 | nsv1063852 | chr21:47317456-47358709 | Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | n/a |
17 | nsv1060235 | chr21:47317456-47360544 | Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | n/a |
18 | nsv914085 | chr21:47342116-47433055 | Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | n/a |
19 | esv1848879 | chr21:47343462-47455584 | Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | n/a |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr21:47333600-47351600 | Weak transcription | Gastric | stomach |
2 | chr21:47340000-47354800 | Weak transcription | Primary T cells from cord blood | blood |
3 | chr21:47343200-47350400 | Weak transcription | Spleen | Spleen |
4 | chr21:47343400-47353800 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
5 | chr21:47343600-47346800 | Weak transcription | Fetal Muscle Leg | muscle |
6 | chr21:47343600-47347400 | Weak transcription | Primary T helper cells fromperipheralblood | blood |
7 | chr21:47343600-47353600 | Weak transcription | Brain Hippocampus Middle | brain |
8 | chr21:47343600-47354600 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
9 | chr21:47346200-47348200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
10 | chr21:47346400-47346600 | Bivalent Enhancer | Fetal Stomach | stomach |