Variant report

Variant	rs11903109
Chromosome Location	chr2:141187809-141187810
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs11884294	0.80[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs11891221	0.82[ASN][1000 genomes]
rs11897270	0.82[ASN][1000 genomes]
rs11899167	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11899434	0.82[ASN][1000 genomes]
rs11903329	0.80[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12999683	0.82[ASN][1000 genomes]
rs13003817	0.82[ASN][1000 genomes]
rs13003819	0.82[ASN][1000 genomes]
rs13003828	0.82[ASN][1000 genomes]
rs13023944	0.82[ASN][1000 genomes]
rs13030114	0.82[ASN][1000 genomes]
rs1401114	0.82[ASN][1000 genomes]
rs1401115	0.82[ASN][1000 genomes]
rs1401117	0.82[ASN][1000 genomes]
rs1518443	0.82[ASN][1000 genomes]
rs1518444	0.82[ASN][1000 genomes]
rs1518445	0.82[ASN][1000 genomes]
rs1518446	0.82[ASN][1000 genomes]
rs17387292	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17387299	0.82[ASN][1000 genomes]
rs17387536	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1829364	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1878741	0.82[ASN][1000 genomes]
rs1878742	0.82[ASN][1000 genomes]
rs4450541	0.90[ASN][1000 genomes]
rs4474828	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6747180	0.82[ASN][1000 genomes]
rs72897813	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72897827	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72897830	0.82[ASN][1000 genomes]
rs72898260	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72898263	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72898290	0.82[ASN][1000 genomes]
rs72899862	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72899866	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72899869	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72899900	0.90[ASN][1000 genomes]
rs72901703	0.90[ASN][1000 genomes]
rs72901708	0.90[ASN][1000 genomes]
rs72901711	0.90[ASN][1000 genomes]
rs72901714	0.90[ASN][1000 genomes]
rs72901718	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72901723	0.90[ASN][1000 genomes]
rs72901724	0.90[ASN][1000 genomes]
rs72901730	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7423992	0.90[ASN][1000 genomes]
rs7593984	0.82[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	esv2754266	chr2:141023643-141270786	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv875186	chr2:141123496-141217244	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
3	esv2756334	chr2:141166521-141285622	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a
4	nsv875187	chr2:141170340-141237995	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:141187600-141188000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:141187600-141188000	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr2:141187600-141188200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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