Variant report

Variant	rs12705623
Chromosome Location	chr7:109287576-109287577
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs11534044	0.88[ASN][1000 genomes]
rs11977707	0.90[ASN][1000 genomes]
rs11978909	0.92[ASN][1000 genomes]
rs12537202	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12705622	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12705624	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12705625	0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12705626	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12705627	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12705628	0.91[ASN][1000 genomes]
rs13233013	0.97[ASN][1000 genomes]
rs13233353	0.98[ASN][1000 genomes]
rs13236909	0.98[ASN][1000 genomes]
rs13241733	0.97[ASN][1000 genomes]
rs13241802	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13242207	0.97[ASN][1000 genomes]
rs13242214	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13242499	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13242591	0.99[ASN][1000 genomes]
rs13243043	0.91[ASN][1000 genomes]
rs13245102	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13245258	0.90[ASN][1000 genomes]
rs13245970	0.97[ASN][1000 genomes]
rs2090429	0.97[ASN][1000 genomes]
rs2090430	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35109891	0.83[ASN][1000 genomes]
rs55873142	0.99[ASN][1000 genomes]
rs6466289	0.97[ASN][1000 genomes]
rs6949527	0.98[ASN][1000 genomes]
rs6951916	0.97[ASN][1000 genomes]
rs6967591	0.92[ASN][1000 genomes]
rs6975819	0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6976113	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7349968	0.98[ASN][1000 genomes]
rs7350020	0.98[ASN][1000 genomes]
rs7784076	0.91[ASN][1000 genomes]
rs7784378	0.93[ASN][1000 genomes]
rs7800655	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023379	chr7:109003574-109355234	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv608079	chr7:109098364-109862289	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1017184	chr7:109240101-109350011	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv981817	chr7:109280619-109303295	Genic enhancers Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:109278800-109300600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr7:109285400-109288200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
3	chr7:109286800-109288200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr7:109287200-109288200	Enhancers	HMEC	breast
5	chr7:109287400-109288400	Enhancers	Hela-S3	cervix

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