Variant report
Variant | rs1718962 |
---|---|
Chromosome Location | chr7:112443049-112443050 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs1017598 | 1.00[AMR][1000 genomes] |
rs1017599 | 1.00[AMR][1000 genomes] |
rs10231221 | 0.81[YRI][hapmap] |
rs10267651 | 1.00[AMR][1000 genomes] |
rs1037299 | 1.00[AMR][1000 genomes] |
rs1227156 | 1.00[AMR][1000 genomes] |
rs1227157 | 1.00[AMR][1000 genomes] |
rs1227160 | 1.00[AMR][1000 genomes] |
rs1227161 | 1.00[AMR][1000 genomes] |
rs1227162 | 1.00[AMR][1000 genomes] |
rs1227165 | 0.84[ASW][hapmap];1.00[AMR][1000 genomes] |
rs1227166 | 1.00[AMR][1000 genomes] |
rs1227167 | 1.00[AMR][1000 genomes] |
rs1227169 | 1.00[AMR][1000 genomes] |
rs1227170 | 0.84[ASW][hapmap];1.00[AMR][1000 genomes] |
rs1227173 | 1.00[AMR][1000 genomes] |
rs1227180 | 1.00[AMR][1000 genomes] |
rs1227186 | 1.00[AMR][1000 genomes] |
rs1227191 | 1.00[AMR][1000 genomes] |
rs1234894 | 1.00[AMR][1000 genomes] |
rs1237908 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs1375856 | 1.00[AMR][1000 genomes] |
rs1449950 | 1.00[AMR][1000 genomes] |
rs1449952 | 1.00[AMR][1000 genomes] |
rs1522630 | 1.00[AMR][1000 genomes] |
rs1620709 | 0.84[ASW][hapmap];1.00[AMR][1000 genomes] |
rs1718933 | 1.00[AMR][1000 genomes] |
rs1718942 | 1.00[AMR][1000 genomes] |
rs1718943 | 1.00[AMR][1000 genomes] |
rs1718953 | 1.00[AMR][1000 genomes] |
rs1718954 | 1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.91[YRI][hapmap];0.81[AFR][1000 genomes] |
rs1718956 | 0.81[AFR][1000 genomes] |
rs1718960 | 0.94[AFR][1000 genomes] |
rs1796496 | 1.00[AMR][1000 genomes] |
rs1796501 | 0.81[AFR][1000 genomes] |
rs1796514 | 0.87[AFR][1000 genomes] |
rs1796515 | 1.00[AMR][1000 genomes] |
rs1830470 | 1.00[AMR][1000 genomes] |
rs1830471 | 1.00[AMR][1000 genomes] |
rs1868586 | 1.00[AMR][1000 genomes] |
rs1976990 | 1.00[AMR][1000 genomes] |
rs2103040 | 1.00[AMR][1000 genomes] |
rs2197953 | 1.00[MKK][hapmap];1.00[AMR][1000 genomes] |
rs2396584 | 1.00[AMR][1000 genomes] |
rs2396585 | 1.00[AMR][1000 genomes] |
rs2396587 | 1.00[AMR][1000 genomes] |
rs2687263 | 1.00[AMR][1000 genomes] |
rs2687265 | 1.00[AMR][1000 genomes] |
rs2687268 | 1.00[AMR][1000 genomes] |
rs2687271 | 1.00[AMR][1000 genomes] |
rs2708294 | 0.82[YRI][hapmap];1.00[AMR][1000 genomes] |
rs2894660 | 1.00[AMR][1000 genomes] |
rs4336532 | 1.00[AMR][1000 genomes] |
rs4727777 | 1.00[AMR][1000 genomes] |
rs501621 | 1.00[MKK][hapmap];0.90[YRI][hapmap];1.00[AMR][1000 genomes] |
rs551461 | 1.00[MKK][hapmap];0.90[YRI][hapmap];1.00[AMR][1000 genomes] |
rs59930732 | 1.00[AMR][1000 genomes] |
rs61390562 | 1.00[AMR][1000 genomes] |
rs637075 | 1.00[AMR][1000 genomes] |
rs6466425 | 1.00[AMR][1000 genomes] |
rs6949796 | 1.00[AMR][1000 genomes] |
rs6950289 | 1.00[AMR][1000 genomes] |
rs7776679 | 1.00[AMR][1000 genomes] |
rs7790704 | 1.00[AMR][1000 genomes] |
rs7790946 | 1.00[AMR][1000 genomes] |
rs7799048 | 1.00[AMR][1000 genomes] |
rs821784 | 0.90[YRI][hapmap];1.00[AMR][1000 genomes] |
rs821786 | 1.00[AMR][1000 genomes] |
rs821788 | 0.90[YRI][hapmap];1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv531436 | chr7:111856171-112585407 | Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 105 gene(s) | inside rSNPs | diseases |
2 | esv2752144 | chr7:112398372-112499924 | ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
3 | esv1794529 | chr7:112400060-112588376 | Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 8 gene(s) | inside rSNPs | diseases |
4 | nsv967494 | chr7:112430613-112445931 | Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | n/a |
5 | nsv1031405 | chr7:112431403-112476756 | Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionmiRNA target site | 2 gene(s) | inside rSNPs | diseases |
6 | nsv429801 | chr7:112434049-112477049 | Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionmiRNA target site | 1 gene(s) | inside rSNPs | diseases |
7 | esv2752145 | chr7:112434049-112500049 | ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionmiRNA target site | 1 gene(s) | inside rSNPs | diseases |
8 | nsv1023222 | chr7:112434413-112476756 | Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionmiRNA target site | 1 gene(s) | inside rSNPs | diseases |
9 | nsv1034863 | chr7:112434413-112504160 | Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionmiRNA target site | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:112442800-112472800 | Weak transcription | Lung | lung |
2 | chr7:112443000-112443200 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |