Variant report
Variant | rs7190716 |
---|---|
Chromosome Location | chr16:10070739-10070740 |
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] |
---|---|
rs10518151 | 1.00[MEX][hapmap] |
rs1070479 | 0.85[CEU][hapmap] |
rs1111537 | 0.81[CEU][hapmap] |
rs11866570 | 1.00[MEX][hapmap] |
rs13331514 | 1.00[MEX][hapmap] |
rs13336632 | 0.82[MEX][hapmap] |
rs1375075 | 1.00[CEU][hapmap] |
rs1448262 | 1.00[MEX][hapmap] |
rs1448268 | 0.81[CEU][hapmap] |
rs1448272 | 0.81[CEU][hapmap] |
rs17569609 | 1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17569693 | 1.00[GIH][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap] |
rs17569940 | 0.81[CEU][hapmap];0.84[EUR][1000 genomes] |
rs17670318 | 1.00[CEU][hapmap];0.94[EUR][1000 genomes] |
rs17670396 | 1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.81[TSI][hapmap];0.96[EUR][1000 genomes] |
rs17670509 | 0.93[EUR][1000 genomes] |
rs17670766 | 0.81[CEU][hapmap];0.84[EUR][1000 genomes] |
rs17671033 | 1.00[MEX][hapmap] |
rs1827197 | 0.81[CEU][hapmap];0.85[EUR][1000 genomes] |
rs2197778 | 0.82[MEX][hapmap] |
rs2315510 | 0.89[CEU][hapmap];0.89[EUR][1000 genomes] |
rs3897996 | 0.84[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs4107019 | 0.81[CEU][hapmap];1.00[MEX][hapmap];0.81[TSI][hapmap];0.85[EUR][1000 genomes] |
rs4254328 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4780784 | 0.81[CEU][hapmap] |
rs4998386 | 1.00[ASW][hapmap];1.00[CEU][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];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57497843 | 0.96[EUR][1000 genomes] |
rs57576479 | 0.91[EUR][1000 genomes] |
rs59775432 | 0.91[EUR][1000 genomes] |
rs60547225 | 0.89[EUR][1000 genomes] |
rs7188291 | 1.00[MEX][hapmap] |
rs7190619 | 0.89[ASW][hapmap];0.90[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap] |
rs7191736 | 1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7192121 | 1.00[CEU][hapmap];0.94[EUR][1000 genomes] |
rs7193123 | 0.85[EUR][1000 genomes] |
rs7193471 | 0.81[EUR][1000 genomes] |
rs7197048 | 0.96[EUR][1000 genomes] |
rs7197200 | 1.00[MEX][hapmap] |
rs7200719 | 0.81[CEU][hapmap];1.00[MEX][hapmap];0.81[TSI][hapmap];0.85[EUR][1000 genomes] |
rs7201627 | 0.81[CEU][hapmap] |
rs7203194 | 1.00[MEX][hapmap] |
rs72772131 | 0.93[EUR][1000 genomes] |
rs72772153 | 0.96[EUR][1000 genomes] |
rs72772155 | 0.96[EUR][1000 genomes] |
rs72772157 | 0.84[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs72772164 | 0.84[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs72772166 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72772167 | 0.93[EUR][1000 genomes] |
rs72772168 | 0.84[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs72772169 | 0.84[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs72772342 | 0.81[EUR][1000 genomes] |
rs72772347 | 0.85[EUR][1000 genomes] |
rs72772360 | 0.81[EUR][1000 genomes] |
rs72772361 | 0.81[EUR][1000 genomes] |
rs72772364 | 0.81[EUR][1000 genomes] |
rs72774046 | 0.86[EUR][1000 genomes] |
rs72774047 | 0.85[EUR][1000 genomes] |
rs72774048 | 0.85[EUR][1000 genomes] |
rs72774051 | 0.85[EUR][1000 genomes] |
rs72774055 | 0.85[EUR][1000 genomes] |
rs72774059 | 0.84[EUR][1000 genomes] |
rs72774081 | 0.85[EUR][1000 genomes] |
rs8043728 | 0.81[CEU][hapmap];1.00[MEX][hapmap];0.81[TSI][hapmap];0.85[EUR][1000 genomes] |
rs8045558 | 1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.81[TSI][hapmap];0.96[EUR][1000 genomes] |
rs8058978 | 1.00[GIH][hapmap] |
rs9302409 | 1.00[MEX][hapmap] |
rs9922383 | 1.00[MEX][hapmap] |
rs9922871 | 1.00[MEX][hapmap] |
rs9925439 | 1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.81[TSI][hapmap];0.94[EUR][1000 genomes] |
rs9929020 | 0.88[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs9930364 | 1.00[MEX][hapmap] |
rs9933111 | 1.00[MEX][hapmap] |
rs9935774 | 1.00[CEU][hapmap] |
Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page:
1
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949196 | chr16:9937980-10182349 | Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | nsv1037001 | chr16:10008023-10476482 | Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
3 | esv2422500 | chr16:10008309-10415517 | Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
4 | nsv1045882 | chr16:10025402-10117992 | Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
5 | nsv1052566 | chr16:10033178-10260068 | Enhancers Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
6 | nsv905333 | chr16:10055461-10079124 | Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
7 | esv2758410 | chr16:10060976-10257550 | Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
8 | esv2758629 | chr16:10060976-10257550 | Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
9 | nsv427973 | chr16:10060976-10257550 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr16:10067800-10072000 | Weak transcription | H9 Cell Line | embryonic stem cell |
2 | chr16:10068600-10071400 | Enhancers | Brain Anterior Caudate | brain |
3 | chr16:10068600-10072000 | Enhancers | Brain Inferior Temporal Lobe | brain |
4 | chr16:10068600-10072000 | Enhancers | Brain Substantia Nigra | brain |
5 | chr16:10068800-10071800 | Weak transcription | GM12878-XiMat | blood |
6 | chr16:10068800-10075000 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
7 | chr16:10069000-10073200 | Enhancers | Brain Cingulate Gyrus | brain |
8 | chr16:10069200-10072400 | Enhancers | Brain Dorsolateral Prefrontal Cortex | brain |
9 | chr16:10069200-10072600 | Enhancers | Brain Angular Gyrus | brain |
10 | chr16:10069200-10073000 | Enhancers | Brain Hippocampus Middle | brain |