Variant report
Variant | rs10011942 |
---|---|
Chromosome Location | chr4:20957155-20957156 |
allele | C/G |
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] |
---|---|
rs10461094 | 0.88[JPT][hapmap];0.90[ASN][1000 genomes] |
rs11727035 | 0.89[ASN][1000 genomes] |
rs13151383 | 0.90[ASN][1000 genomes] |
rs1347385 | 0.81[CHB][hapmap];0.87[JPT][hapmap];0.85[ASN][1000 genomes] |
rs1352796 | 0.87[JPT][hapmap] |
rs1388326 | 0.81[CHB][hapmap];0.83[JPT][hapmap] |
rs1434943 | 0.80[CEU][hapmap] |
rs1434946 | 0.96[ASN][1000 genomes] |
rs1434950 | 0.81[CHB][hapmap];0.87[JPT][hapmap];0.90[ASN][1000 genomes] |
rs1491356 | 0.87[JPT][hapmap] |
rs1491357 | 0.87[JPT][hapmap] |
rs1491361 | 0.88[JPT][hapmap] |
rs1565534 | 0.87[JPT][hapmap] |
rs1836520 | 0.90[ASN][1000 genomes] |
rs1865444 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes] |
rs4395501 | 0.81[CHB][hapmap];0.87[JPT][hapmap];0.90[ASN][1000 genomes] |
rs4441750 | 0.81[CHB][hapmap];0.90[ASN][1000 genomes] |
rs4696968 | 0.81[ASN][1000 genomes] |
rs4697196 | 0.84[ASN][1000 genomes] |
rs6447998 | 0.82[JPT][hapmap] |
rs6447999 | 0.81[CHB][hapmap];0.82[JPT][hapmap] |
rs6448003 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes] |
rs6448004 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes] |
rs6811024 | 0.83[JPT][hapmap] |
rs6836783 | 0.84[ASN][1000 genomes] |
rs6843757 | 0.81[CHB][hapmap];0.87[JPT][hapmap] |
rs6858759 | 0.81[CHB][hapmap];0.87[JPT][hapmap];0.89[ASN][1000 genomes] |
rs7677635 | 0.81[CHB][hapmap];0.87[JPT][hapmap];0.90[ASN][1000 genomes] |
rs7677781 | 0.87[JPT][hapmap] |
rs7690016 | 0.81[CHB][hapmap];0.87[JPT][hapmap] |
rs980276 | 0.82[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1010145 | chr4:20601908-21057992 | ZNF genes & repeats Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 6 gene(s) | inside rSNPs | diseases |
2 | nsv537052 | chr4:20601908-21057992 | Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 6 gene(s) | inside rSNPs | diseases |
3 | nsv1014941 | chr4:20611726-21345226 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
4 | nsv537053 | chr4:20611726-21345226 | ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
5 | nsv1013365 | chr4:20834054-21609078 | Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
6 | nsv829877 | chr4:20847465-20992544 | Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:20945600-20959600 | Weak transcription | Colon Smooth Muscle | Colon |
2 | chr4:20956800-20960400 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |