Variant report

Variant	rs4695991
Chromosome Location	chr4:173645762-173645763
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10520242	0.83[EUR][1000 genomes]
rs11132959	0.86[EUR][1000 genomes]
rs12499966	0.96[EUR][1000 genomes]
rs12502034	0.96[EUR][1000 genomes]
rs12502278	1.00[CEU][hapmap]
rs12505471	0.96[EUR][1000 genomes]
rs12509227	0.96[EUR][1000 genomes]
rs12510199	1.00[CEU][hapmap]
rs12510770	0.96[EUR][1000 genomes]
rs12510844	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12511707	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12511715	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12643395	0.90[EUR][1000 genomes]
rs12645440	0.95[EUR][1000 genomes]
rs12651320	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1437828	0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1437840	1.00[CEU][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1455130	1.00[CEU][hapmap]
rs1540471	1.00[CEU][hapmap]
rs1540472	0.83[EUR][1000 genomes]
rs1551664	1.00[CEU][hapmap]
rs1551665	1.00[CEU][hapmap]
rs17058683	0.84[EUR][1000 genomes]
rs17058705	1.00[CEU][hapmap];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17058736	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17058882	1.00[CEU][hapmap]
rs1946797	0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2043781	1.00[CEU][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2099606	1.00[CEU][hapmap]
rs2118441	0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2125601	1.00[CEU][hapmap]
rs36081927	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4522845	0.96[EUR][1000 genomes]
rs4695932	0.83[EUR][1000 genomes]
rs4696014	0.96[EUR][1000 genomes]
rs4696032	1.00[CEU][hapmap]
rs58774009	0.91[EUR][1000 genomes]
rs61077359	0.82[EUR][1000 genomes]
rs62330792	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62330815	0.96[EUR][1000 genomes]
rs62330816	0.96[EUR][1000 genomes]
rs62330818	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62330819	0.96[EUR][1000 genomes]
rs62330820	0.96[EUR][1000 genomes]
rs6812449	0.96[EUR][1000 genomes]
rs6821734	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6822579	0.86[EUR][1000 genomes]
rs6838201	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs747493	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7664183	0.96[EUR][1000 genomes]
rs7694886	0.96[EUR][1000 genomes]
rs837196	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:173645200-173649600	Enhancers	Fetal Intestine Small	intestine
2	chr4:173645400-173646400	Enhancers	A549	lung
3	chr4:173645600-173647000	Enhancers	Fetal Intestine Large	intestine

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