Variant report

Variant	rs4682017
Chromosome Location	chr3:110396181-110396182
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 100 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs10934055	0.90[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10934056	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10934063	0.84[AMR][1000 genomes]
rs10934064	0.86[AMR][1000 genomes]
rs1156330	0.81[ASN][1000 genomes]
rs1156778	0.86[ASN][1000 genomes]
rs12493010	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1398352	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1462294	0.82[ASN][1000 genomes]
rs1462302	0.81[ASN][1000 genomes]
rs1462303	0.81[ASN][1000 genomes]
rs1462316	0.84[ASN][1000 genomes]
rs1473828	0.85[ASN][1000 genomes]
rs1512522	0.85[ASN][1000 genomes]
rs1512524	0.85[ASN][1000 genomes]
rs1512530	0.84[ASN][1000 genomes]
rs1547543	0.85[ASN][1000 genomes]
rs1585559	0.80[ASN][1000 genomes]
rs1599569	0.82[ASN][1000 genomes]
rs1824630	0.84[ASN][1000 genomes]
rs1903678	0.84[ASN][1000 genomes]
rs1913090	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1913091	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2055965	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2199454	0.82[ASN][1000 genomes]
rs2399356	0.84[ASN][1000 genomes]
rs2399361	0.80[ASN][1000 genomes]
rs4234400	0.85[ASN][1000 genomes]
rs4362750	0.86[ASN][1000 genomes]
rs4395426	0.85[ASN][1000 genomes]
rs4410465	0.85[ASN][1000 genomes]
rs4438690	0.84[ASN][1000 genomes]
rs4449350	0.85[ASN][1000 genomes]
rs4450854	0.85[ASN][1000 genomes]
rs4469006	0.85[ASN][1000 genomes]
rs4481181	0.84[ASN][1000 genomes]
rs4547734	0.84[ASN][1000 genomes]
rs4550849	0.83[ASN][1000 genomes]
rs4588395	0.85[ASN][1000 genomes]
rs4634158	0.83[ASN][1000 genomes]
rs4682014	0.85[ASN][1000 genomes]
rs4682018	0.86[ASN][1000 genomes]
rs4682192	0.85[ASN][1000 genomes]
rs4682193	0.85[ASN][1000 genomes]
rs4682194	0.85[ASN][1000 genomes]
rs4682195	0.85[ASN][1000 genomes]
rs4682198	0.86[ASN][1000 genomes]
rs55894328	0.83[ASN][1000 genomes]
rs60302938	0.84[AMR][1000 genomes]
rs62270121	0.84[AMR][1000 genomes]
rs62270122	0.84[AMR][1000 genomes]
rs62270123	0.84[AMR][1000 genomes]
rs62270127	0.84[AMR][1000 genomes]
rs62270130	0.84[AMR][1000 genomes]
rs62271763	0.84[AMR][1000 genomes]
rs6762150	0.81[ASN][1000 genomes]
rs6768474	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6772035	0.84[AMR][1000 genomes]
rs6773268	0.80[ASN][1000 genomes]
rs6776067	0.84[AMR][1000 genomes]
rs6784490	0.85[ASN][1000 genomes]
rs7615772	0.82[ASN][1000 genomes]
rs7632974	0.84[AMR][1000 genomes]
rs7637105	0.85[ASN][1000 genomes]
rs7650722	0.84[AMR][1000 genomes]
rs7652062	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9816253	0.81[ASN][1000 genomes]
rs9825259	0.84[AMR][1000 genomes]
rs9826294	0.84[ASN][1000 genomes]
rs9830959	0.81[ASN][1000 genomes]
rs9838550	0.86[ASN][1000 genomes]
rs9838611	0.85[ASN][1000 genomes]
rs9838715	0.85[ASN][1000 genomes]
rs9840671	0.85[ASN][1000 genomes]
rs9842924	0.84[ASN][1000 genomes]
rs9843528	0.85[ASN][1000 genomes]
rs9843978	0.85[ASN][1000 genomes]
rs9844791	0.85[ASN][1000 genomes]
rs9857065	0.80[ASN][1000 genomes]
rs9858359	0.84[AMR][1000 genomes]
rs986205	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs986206	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9863549	0.85[ASN][1000 genomes]
rs9873714	0.84[AMR][1000 genomes]
rs9874241	0.85[ASN][1000 genomes]
rs9876058	0.85[ASN][1000 genomes]
rs9884058	0.84[ASN][1000 genomes]
rs991930	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv520365	chr3:110155172-110441165	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1001144	chr3:110158316-110431113	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv536687	chr3:110158316-110431113	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1001810	chr3:110158316-110522247	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1010230	chr3:110204439-110588814	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv536688	chr3:110204439-110588814	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1011034	chr3:110209344-110559021	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv536689	chr3:110209344-110559021	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv1003106	chr3:110264476-111105943	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
10	nsv1014199	chr3:110293896-110754155	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
11	nsv829673	chr3:110378069-110530815	Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	nsv3941	chr3:110385790-110430523	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:110391200-110398000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:110391400-110398000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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