Variant report
Variant | rs1269602 |
---|---|
Chromosome Location | chr10:116941272-116941273 |
allele | A/G |
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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No data |
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rs_ID | r2[population] |
---|---|
rs10787554 | 0.95[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs10787555 | 0.97[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10787557 | 0.80[EUR][1000 genomes] |
rs10787558 | 0.85[EUR][1000 genomes] |
rs10885649 | 0.81[EUR][1000 genomes] |
rs10885651 | 0.88[EUR][1000 genomes] |
rs10885655 | 0.89[EUR][1000 genomes] |
rs10885657 | 0.82[EUR][1000 genomes] |
rs10885658 | 0.92[EUR][1000 genomes] |
rs10885659 | 0.91[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs10885660 | 0.91[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs10885662 | 0.91[EUR][1000 genomes] |
rs10885664 | 0.80[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs10885669 | 0.95[EUR][1000 genomes] |
rs10885671 | 0.94[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10885672 | 0.94[EUR][1000 genomes] |
rs10885673 | 0.98[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10885675 | 0.97[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs10885676 | 0.93[EUR][1000 genomes] |
rs10885677 | 0.91[EUR][1000 genomes] |
rs10885680 | 0.88[EUR][1000 genomes] |
rs10885681 | 0.89[EUR][1000 genomes] |
rs10885682 | 0.84[EUR][1000 genomes] |
rs10885683 | 0.88[EUR][1000 genomes] |
rs11197066 | 0.86[EUR][1000 genomes] |
rs11197071 | 0.86[EUR][1000 genomes] |
rs11197081 | 0.91[EUR][1000 genomes] |
rs11197084 | 0.94[EUR][1000 genomes] |
rs11197087 | 0.91[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs11197091 | 0.91[EUR][1000 genomes] |
rs11197093 | 0.92[ASN][1000 genomes] |
rs11197094 | 0.93[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs11197103 | 0.80[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs11197107 | 0.96[EUR][1000 genomes] |
rs11197110 | 0.95[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs11197122 | 0.94[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs11197126 | 0.97[EUR][1000 genomes] |
rs11197127 | 0.97[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs11197139 | 0.94[EUR][1000 genomes] |
rs11197149 | 0.85[EUR][1000 genomes] |
rs11197150 | 0.85[EUR][1000 genomes] |
rs11197159 | 0.88[EUR][1000 genomes] |
rs11197160 | 0.83[EUR][1000 genomes] |
rs11197168 | 0.83[EUR][1000 genomes] |
rs11517121 | 0.84[EUR][1000 genomes] |
rs11525277 | 0.89[EUR][1000 genomes] |
rs11527959 | 0.80[EUR][1000 genomes] |
rs12218100 | 0.93[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs12218477 | 0.83[EUR][1000 genomes] |
rs12355617 | 0.89[EUR][1000 genomes] |
rs12357053 | 0.85[EUR][1000 genomes] |
rs12358411 | 0.94[EUR][1000 genomes] |
rs12360503 | 0.94[EUR][1000 genomes] |
rs12573443 | 0.96[EUR][1000 genomes] |
rs1264748 | 0.86[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1264756 | 0.85[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs1264763 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs1264765 | 0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1264768 | 0.85[EUR][1000 genomes] |
rs1264794 | 0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1264795 | 0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1264796 | 0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1264802 | 0.89[EUR][1000 genomes] |
rs1268459 | 0.81[ASN][1000 genomes] |
rs1268460 | 0.81[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs1268916 | 0.84[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1270442 | 0.82[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs1537685 | 0.91[EUR][1000 genomes] |
rs17092908 | 0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs17722681 | 0.92[EUR][1000 genomes] |
rs1899718 | 0.94[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1899721 | 0.99[EUR][1000 genomes] |
rs2050705 | 0.80[EUR][1000 genomes] |
rs2152148 | 0.89[EUR][1000 genomes] |
rs2172669 | 0.88[EUR][1000 genomes] |
rs2256046 | 0.93[EUR][1000 genomes] |
rs2265930 | 0.82[EUR][1000 genomes] |
rs2420075 | 0.91[EUR][1000 genomes] |
rs2420077 | 0.85[EUR][1000 genomes] |
rs2420078 | 0.82[EUR][1000 genomes] |
rs2440313 | 0.96[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs2492980 | 0.81[EUR][1000 genomes] |
rs2492981 | 0.84[EUR][1000 genomes] |
rs34938864 | 0.83[EUR][1000 genomes] |
rs35120367 | 0.90[EUR][1000 genomes] |
rs35728982 | 0.89[EUR][1000 genomes] |
rs4752724 | 0.95[EUR][1000 genomes] |
rs61880825 | 0.88[EUR][1000 genomes] |
rs7474585 | 0.98[EUR][1000 genomes] |
rs7912050 | 0.80[EUR][1000 genomes] |
rs923907 | 0.85[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3435429 | chr10:116394152-117006347 | Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 21 gene(s) | inside rSNPs | diseases |
2 | nsv831998 | chr10:116847998-116969618 | Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
3 | nsv869279 | chr10:116884639-117032437 | Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv868940 | chr10:116933802-117032437 | Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | esv3424905 | chr10:116941162-116945560 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:116926600-116951400 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |