Variant report
Variant | rs9326105 |
---|---|
Chromosome Location | chr1:73189021-73189022 |
allele | A/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr1:73181346..73184286-chr1:73186090..73189025,2 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000212366 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10465865 | 1.00[ASN][1000 genomes] |
rs10465866 | 1.00[ASN][1000 genomes] |
rs10889969 | 1.00[ASN][1000 genomes] |
rs10889976 | 1.00[ASN][1000 genomes] |
rs10889981 | 1.00[ASN][1000 genomes] |
rs11209987 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11209989 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11209993 | 1.00[ASN][1000 genomes] |
rs11209997 | 1.00[ASN][1000 genomes] |
rs11209998 | 1.00[ASN][1000 genomes] |
rs11210000 | 1.00[ASN][1000 genomes] |
rs11210001 | 1.00[ASN][1000 genomes] |
rs11210002 | 1.00[ASN][1000 genomes] |
rs11210015 | 0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11210016 | 1.00[ASN][1000 genomes] |
rs11210018 | 1.00[ASN][1000 genomes] |
rs11210019 | 1.00[ASN][1000 genomes] |
rs11210021 | 1.00[ASN][1000 genomes] |
rs11210022 | 1.00[ASN][1000 genomes] |
rs11210028 | 1.00[ASN][1000 genomes] |
rs11210036 | 1.00[ASN][1000 genomes] |
rs11210042 | 0.89[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11803059 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11807168 | 1.00[ASN][1000 genomes] |
rs12062883 | 1.00[ASN][1000 genomes] |
rs12066284 | 1.00[ASN][1000 genomes] |
rs12066923 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12070137 | 1.00[ASN][1000 genomes] |
rs12072129 | 1.00[ASN][1000 genomes] |
rs12072443 | 1.00[ASN][1000 genomes] |
rs12072444 | 1.00[ASN][1000 genomes] |
rs12073769 | 1.00[ASN][1000 genomes] |
rs12073811 | 1.00[ASN][1000 genomes] |
rs12076822 | 1.00[ASN][1000 genomes] |
rs12078724 | 1.00[ASN][1000 genomes] |
rs12082218 | 1.00[ASN][1000 genomes] |
rs12082422 | 0.99[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12087633 | 1.00[ASN][1000 genomes] |
rs12087817 | 1.00[ASN][1000 genomes] |
rs12088885 | 1.00[ASN][1000 genomes] |
rs12092131 | 1.00[ASN][1000 genomes] |
rs12092187 | 1.00[ASN][1000 genomes] |
rs13352999 | 1.00[ASN][1000 genomes] |
rs1373915 | 1.00[ASN][1000 genomes] |
rs17093152 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17093160 | 1.00[ASN][1000 genomes] |
rs17093164 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17093275 | 1.00[ASN][1000 genomes] |
rs17093297 | 0.99[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17093299 | 1.00[ASN][1000 genomes] |
rs17093396 | 1.00[ASN][1000 genomes] |
rs2017920 | 1.00[ASN][1000 genomes] |
rs2244679 | 1.00[ASN][1000 genomes] |
rs2244685 | 1.00[ASN][1000 genomes] |
rs2244943 | 1.00[ASN][1000 genomes] |
rs2255220 | 1.00[ASN][1000 genomes] |
rs2255572 | 1.00[ASN][1000 genomes] |
rs2255605 | 1.00[ASN][1000 genomes] |
rs2255606 | 1.00[ASN][1000 genomes] |
rs2255692 | 1.00[ASN][1000 genomes] |
rs2255706 | 1.00[ASN][1000 genomes] |
rs2590940 | 1.00[ASN][1000 genomes] |
rs2841184 | 1.00[ASN][1000 genomes] |
rs28416453 | 1.00[ASN][1000 genomes] |
rs28464217 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34236777 | 1.00[ASN][1000 genomes] |
rs4595322 | 1.00[ASN][1000 genomes] |
rs4650141 | 1.00[ASN][1000 genomes] |
rs56690886 | 1.00[ASN][1000 genomes] |
rs57867136 | 1.00[ASN][1000 genomes] |
rs59526352 | 1.00[ASN][1000 genomes] |
rs60276726 | 1.00[ASN][1000 genomes] |
rs61138734 | 0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61224710 | 1.00[ASN][1000 genomes] |
rs61464630 | 0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6657668 | 1.00[ASN][1000 genomes] |
rs6690920 | 1.00[ASN][1000 genomes] |
rs72942866 | 1.00[ASN][1000 genomes] |
rs72942886 | 0.89[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs72942900 | 1.00[ASN][1000 genomes] |
rs72944803 | 1.00[ASN][1000 genomes] |
rs72946915 | 1.00[ASN][1000 genomes] |
rs72948923 | 1.00[ASN][1000 genomes] |
rs74090123 | 1.00[EUR][1000 genomes] |
rs7521173 | 1.00[ASN][1000 genomes] |
rs7536612 | 1.00[ASN][1000 genomes] |
rs9326103 | 1.00[ASN][1000 genomes] |
rs9326104 | 1.00[ASN][1000 genomes] |
rs986381 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv428101 | chr1:73017520-73211351 | Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | nsv871636 | chr1:73048685-73274919 | ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv871181 | chr1:73084221-73305593 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
4 | esv2757735 | chr1:73181612-73307170 | Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
5 | esv2758941 | chr1:73181612-73307170 | Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Weak transcription | TF binding regionChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
6 | esv3331895 | chr1:73183764-73189062 | Inactive region | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
No data |