Variant report

Variant	rs11132954
Chromosome Location	chr4:173607221-173607222
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 112 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:104)

rs_ID	r²[population]
rs10001933	0.92[CEU][hapmap]
rs10016145	0.84[JPT][hapmap]
rs10024969	0.86[CHB][hapmap];0.85[JPT][hapmap]
rs10520242	0.86[CHB][hapmap];0.84[JPT][hapmap]
rs10866355	0.85[ASN][1000 genomes]
rs10866361	0.84[JPT][hapmap]
rs10866362	0.85[JPT][hapmap]
rs10866364	0.81[JPT][hapmap]
rs1106651	0.86[ASN][1000 genomes]
rs11132955	0.84[JPT][hapmap]
rs11132959	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.97[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1158684	0.82[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs11722378	0.82[ASN][1000 genomes]
rs11938551	0.84[JPT][hapmap]
rs12499966	0.80[EUR][1000 genomes]
rs12501331	0.87[ASN][1000 genomes]
rs12502034	0.80[EUR][1000 genomes]
rs12505471	0.80[EUR][1000 genomes]
rs12509227	0.80[EUR][1000 genomes]
rs12510770	0.80[EUR][1000 genomes]
rs12511707	0.84[CHB][hapmap];0.84[JPT][hapmap];0.80[EUR][1000 genomes]
rs12513314	0.86[CHB][hapmap];0.84[JPT][hapmap]
rs12643395	0.82[CHB][hapmap];0.85[JPT][hapmap]
rs12643816	0.86[CHB][hapmap]
rs12647340	1.00[JPT][hapmap]
rs12649426	1.00[JPT][hapmap]
rs12651320	0.86[CHB][hapmap];0.84[JPT][hapmap]
rs13107045	0.82[ASN][1000 genomes]
rs13134194	0.84[JPT][hapmap]
rs13146563	1.00[JPT][hapmap]
rs1347698	0.91[CHB][hapmap];0.84[JPT][hapmap]
rs1347700	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs1347702	0.81[CHB][hapmap];0.84[JPT][hapmap]
rs1370581	0.82[ASN][1000 genomes]
rs1437828	0.81[EUR][1000 genomes]
rs1437834	0.95[JPT][hapmap]
rs1437837	0.95[JPT][hapmap]
rs1437842	0.82[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs1540466	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap]
rs1540468	0.86[CHB][hapmap];0.84[JPT][hapmap]
rs1540470	0.94[JPT][hapmap]
rs1540472	0.81[CHB][hapmap];0.84[JPT][hapmap]
rs1548346	0.82[CHB][hapmap];0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs17058683	0.82[CHB][hapmap]
rs17058736	0.81[CHB][hapmap]
rs17058752	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs17058802	0.86[CHB][hapmap]
rs17307651	0.82[CHB][hapmap];0.89[JPT][hapmap]
rs17308839	0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs17308944	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs1898554	0.83[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs1946797	0.86[CHB][hapmap];0.84[JPT][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2043783	0.84[JPT][hapmap]
rs2118439	0.84[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs2118441	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2118442	0.82[ASN][1000 genomes]
rs34567973	0.82[ASN][1000 genomes]
rs35184155	0.82[ASN][1000 genomes]
rs35280724	0.82[ASN][1000 genomes]
rs35345168	0.82[ASN][1000 genomes]
rs36081927	0.80[EUR][1000 genomes]
rs4470604	0.82[CHB][hapmap];0.94[JPT][hapmap]
rs4476577	0.80[JPT][hapmap]
rs4522845	0.90[CHB][hapmap];0.80[EUR][1000 genomes]
rs4546224	0.84[JPT][hapmap]
rs4569731	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap]
rs4608790	0.86[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs4695771	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs4695799	0.86[CHB][hapmap];0.94[JPT][hapmap]
rs4695932	0.84[JPT][hapmap]
rs4696006	0.83[CHB][hapmap];0.95[JPT][hapmap]
rs4696014	0.90[CHB][hapmap];0.80[EUR][1000 genomes]
rs4696015	0.82[ASN][1000 genomes]
rs4696016	0.82[ASN][1000 genomes]
rs4696022	0.85[JPT][hapmap]
rs4696029	0.92[CEU][hapmap]
rs4696031	0.84[CEU][hapmap]
rs55850929	0.81[ASN][1000 genomes]
rs62330815	0.80[EUR][1000 genomes]
rs62330816	0.80[EUR][1000 genomes]
rs62330819	0.80[EUR][1000 genomes]
rs62330820	0.80[EUR][1000 genomes]
rs6553645	0.82[ASN][1000 genomes]
rs6553658	0.85[JPT][hapmap]
rs6812449	0.80[EUR][1000 genomes]
rs6819441	0.82[ASN][1000 genomes]
rs6822571	0.83[CHB][hapmap];0.90[JPT][hapmap]
rs6822579	0.97[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6827154	0.90[CHB][hapmap];0.84[JPT][hapmap]
rs6838201	0.80[EUR][1000 genomes]
rs6844200	0.90[CHB][hapmap]
rs6855645	0.82[CHB][hapmap];0.94[JPT][hapmap]
rs6858309	0.80[JPT][hapmap]
rs7438724	0.83[JPT][hapmap]
rs748347	1.00[JPT][hapmap]
rs7659511	1.00[JPT][hapmap]
rs7664183	0.80[EUR][1000 genomes]
rs7672787	0.82[ASN][1000 genomes]
rs7676941	0.92[CEU][hapmap]
rs7681059	0.92[CEU][hapmap]
rs7691448	0.82[ASN][1000 genomes]
rs7694886	0.80[EUR][1000 genomes]
rs837196	0.86[CHB][hapmap];0.84[JPT][hapmap]
rs9312527	0.86[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031592	chr4:173112542-173662991	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv537359	chr4:173112542-173662991	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv948856	chr4:173388217-173967546	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv949126	chr4:173466221-174051451	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv880685	chr4:173562564-173661711	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv880613	chr4:173569281-173661711	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	esv3327952	chr4:173591786-173805861	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv968024	chr4:173604337-173609980	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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