Variant report
Variant | rs9987891 |
---|---|
Chromosome Location | chr9:10327533-10327534 |
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] |
---|---|
rs10122293 | 0.84[CEU][hapmap] |
rs10123173 | 0.90[EUR][1000 genomes] |
rs10123946 | 0.84[CEU][hapmap] |
rs10756023 | 0.80[CHB][hapmap];0.88[JPT][hapmap] |
rs10756025 | 0.93[EUR][1000 genomes] |
rs10756027 | 0.89[CEU][hapmap] |
rs10756028 | 0.82[EUR][1000 genomes] |
rs10809061 | 0.86[CHB][hapmap];0.88[JPT][hapmap] |
rs10959014 | 0.89[CEU][hapmap] |
rs10959016 | 0.83[CEU][hapmap] |
rs10959026 | 0.89[CEU][hapmap] |
rs10959043 | 0.89[EUR][1000 genomes] |
rs10959045 | 0.95[CEU][hapmap];0.94[EUR][1000 genomes] |
rs10959050 | 0.80[CEU][hapmap] |
rs10959051 | 0.80[CEU][hapmap] |
rs12344926 | 0.83[CEU][hapmap] |
rs12345848 | 0.81[CHB][hapmap];0.88[JPT][hapmap] |
rs1323498 | 0.89[CEU][hapmap] |
rs1323500 | 0.89[CEU][hapmap] |
rs1407925 | 0.89[CEU][hapmap] |
rs1535663 | 0.81[CEU][hapmap] |
rs1924084 | 0.93[EUR][1000 genomes] |
rs592682 | 0.86[CHB][hapmap];0.88[JPT][hapmap] |
rs603924 | 0.92[YRI][hapmap] |
rs616040 | 0.89[CEU][hapmap] |
rs616951 | 0.87[YRI][hapmap] |
rs633062 | 0.84[CEU][hapmap] |
rs635580 | 0.93[CHB][hapmap];1.00[JPT][hapmap] |
rs635925 | 0.93[CHB][hapmap];0.88[JPT][hapmap] |
rs684853 | 0.80[CHB][hapmap];0.88[JPT][hapmap] |
rs694201 | 0.89[CEU][hapmap] |
rs694209 | 0.89[CEU][hapmap] |
rs7849722 | 0.80[CEU][hapmap] |
rs7851619 | 0.81[EUR][1000 genomes] |
rs7854874 | 0.92[EUR][1000 genomes] |
rs7856548 | 0.93[CHB][hapmap];0.89[JPT][hapmap] |
rs880634 | 0.89[CEU][hapmap] |
rs942158 | 0.89[CEU][hapmap] |
rs9657580 | 0.89[CEU][hapmap];0.89[EUR][1000 genomes] |
rs9987444 | 0.93[EUR][1000 genomes] |
rs9987798 | 0.89[CEU][hapmap];0.90[EUR][1000 genomes] |
rs9987808 | 0.90[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1034731 | chr9:9776126-10481262 | Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv892295 | chr9:9832245-10380406 | Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv1030657 | chr9:10002355-10481262 | Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
4 | nsv1033178 | chr9:10169848-10428731 | Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | esv2758179 | chr9:10188450-10370398 | Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | esv2759666 | chr9:10188450-10370398 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
7 | nsv1033020 | chr9:10314941-10330352 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
8 | esv2764134 | chr9:10314941-10330364 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
9 | nsv516073 | chr9:10314941-10333382 | Enhancers Weak transcription Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:10323600-10330200 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
2 | chr9:10325400-10330800 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
3 | chr9:10325400-10331200 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
4 | chr9:10325800-10331200 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
5 | chr9:10325800-10335800 | Weak transcription | HUES64 Cell Line | embryonic stem cell |