Variant report

Variant	rs13023944
Chromosome Location	chr2:141193126-141193127
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs11884294	1.00[JPT][hapmap]
rs11891221	0.84[CEU][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11895957	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11897270	1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11898162	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11899167	0.82[ASN][1000 genomes]
rs11899434	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11901300	0.82[ASN][1000 genomes]
rs11903109	0.82[ASN][1000 genomes]
rs11903329	1.00[JPT][hapmap]
rs12999683	0.84[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13003817	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13003819	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13003828	0.83[CEU][hapmap];0.87[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13030091	0.86[EUR][1000 genomes]
rs13030114	0.84[CEU][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13422213	1.00[JPT][hapmap]
rs1401114	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1401115	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1401117	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs1518440	1.00[JPT][hapmap]
rs1518443	0.83[CEU][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1518444	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs1518445	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs1518446	0.84[CEU][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1607387	1.00[JPT][hapmap]
rs17387292	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs17387299	0.84[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17387536	0.82[ASN][1000 genomes]
rs17478629	1.00[JPT][hapmap]
rs1878741	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs1878742	0.80[CEU][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs41323147	1.00[JPT][hapmap]
rs41478345	1.00[JPT][hapmap]
rs4293513	0.80[CEU][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs4450541	1.00[JPT][hapmap]
rs4474828	0.82[ASN][1000 genomes]
rs6747180	0.83[CEU][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72895991	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs72897813	0.82[ASN][1000 genomes]
rs72897827	0.82[ASN][1000 genomes]
rs72897830	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72898290	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72899862	0.82[ASN][1000 genomes]
rs72899866	0.82[ASN][1000 genomes]
rs72899869	0.82[ASN][1000 genomes]
rs72901730	0.82[ASN][1000 genomes]
rs7422845	1.00[JPT][hapmap]
rs7581949	1.00[JPT][hapmap]
rs7593984	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[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:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:141188000-141193200	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr2:141193000-141193200	Enhancers	Fetal Lung	lung
3	chr2:141193000-141193400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr2:141193000-141193400	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr2:141193000-141193600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
6	chr2:141193000-141193600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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