Variant report
Variant | rs338999 |
---|---|
Chromosome Location | chr3:120970900-120970901 |
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] |
---|---|
rs1108170 | 0.88[ASN][1000 genomes] |
rs1191289 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs1191291 | 0.87[AFR][1000 genomes];0.84[ASN][1000 genomes] |
rs1191292 | 0.80[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1191294 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1191298 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs1191299 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1191302 | 0.85[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs1191307 | 0.85[AFR][1000 genomes];0.80[ASN][1000 genomes] |
rs1191308 | 0.85[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs1211857 | 0.82[ASN][1000 genomes] |
rs13318249 | 0.80[ASN][1000 genomes] |
rs1504538 | 0.81[ASN][1000 genomes] |
rs1518597 | 0.80[ASN][1000 genomes] |
rs1546347 | 0.93[AFR][1000 genomes];0.93[ASN][1000 genomes] |
rs16832125 | 0.85[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs170939 | 0.81[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs1795384 | 0.97[AFR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1795391 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs1795393 | 0.83[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs191438 | 0.94[AFR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs1920547 | 0.83[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs2175453 | 0.86[ASN][1000 genomes] |
rs2331538 | 0.80[ASN][1000 genomes] |
rs2331642 | 0.82[ASN][1000 genomes] |
rs2331710 | 0.93[AFR][1000 genomes];0.88[ASN][1000 genomes] |
rs234996 | 0.86[AFR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs2679284 | 0.85[AFR][1000 genomes];0.87[ASN][1000 genomes] |
rs2679286 | 0.83[AFR][1000 genomes] |
rs2701052 | 0.87[ASN][1000 genomes] |
rs338957 | 0.97[AFR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs338970 | 0.81[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs338971 | 0.84[AFR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs338974 | 0.90[AFR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs338975 | 0.81[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs338978 | 0.94[AFR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs338980 | 0.81[AFR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs338984 | 0.98[AFR][1000 genomes];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs338987 | 0.99[AFR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs338988 | 0.96[AFR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs338989 | 0.98[AFR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs338990 | 0.83[AFR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs338993 | 0.81[AFR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs338995 | 0.88[AFR][1000 genomes];0.93[ASN][1000 genomes] |
rs338998 | 0.81[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs339002 | 0.84[AFR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs339004 | 0.83[AFR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs339007 | 0.81[AFR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs339008 | 0.98[AFR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs339009 | 0.98[AFR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs3908117 | 0.80[ASN][1000 genomes] |
rs4676710 | 0.82[ASN][1000 genomes] |
rs6781737 | 0.89[ASN][1000 genomes] |
rs6782749 | 0.80[ASN][1000 genomes] |
rs6787064 | 0.85[ASN][1000 genomes] |
rs6793427 | 0.88[ASN][1000 genomes] |
rs6800080 | 0.81[ASN][1000 genomes] |
rs7621325 | 0.85[ASN][1000 genomes] |
rs7636533 | 0.89[AFR][1000 genomes];0.84[ASN][1000 genomes] |
rs7637100 | 0.89[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs9332451 | 0.93[AFR][1000 genomes];0.88[ASN][1000 genomes] |
rs9827406 | 0.82[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv869548 | chr3:120320731-121076337 | Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 25 gene(s) | inside rSNPs | diseases |
2 | nsv916869 | chr3:120360281-120973169 | Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
3 | nsv1005275 | chr3:120700604-121102735 | Strong transcription ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
4 | nsv998555 | chr3:120700604-121348015 | Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 19 gene(s) | inside rSNPs | diseases |
5 | nsv1008441 | chr3:120730017-121102735 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
6 | nsv536709 | chr3:120730017-121102735 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
7 | nsv1005525 | chr3:120749594-121027161 | ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 3 gene(s) | inside rSNPs | diseases |
8 | nsv1012777 | chr3:120883846-120974864 | Enhancers Strong transcription Active TSS ZNF genes & repeats Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
9 | nsv829701 | chr3:120935402-121115932 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
10 | nsv517501 | chr3:120941578-120970900 | Enhancers Weak transcription Strong transcription ZNF genes & repeats | n/a | n/a | inside rSNPs | diseases |
11 | nsv518828 | chr3:120941578-120977383 | Enhancers Strong transcription Weak transcription ZNF genes & repeats | n/a | n/a | inside rSNPs | diseases |
12 | nsv521397 | chr3:120970900-121192350 | Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
13 | nsv591395 | chr3:120970900-121501070 | Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 47 gene(s) | inside rSNPs | diseases |
14 | nsv591396 | chr3:120970900-121557533 | Strong transcription Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 50 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:120962000-120993000 | Weak transcription | Ovary | ovary |