Variant report

Variant	rs3765639
Chromosome Location	chr4:74347771-74347772
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10028196	0.80[ASN][1000 genomes]
rs10212657	0.82[ASN][1000 genomes]
rs10213305	0.82[ASN][1000 genomes]
rs10805065	0.81[ASN][1000 genomes]
rs10938075	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10938077	0.81[ASN][1000 genomes]
rs10938078	0.81[ASN][1000 genomes]
rs10938079	0.81[ASN][1000 genomes]
rs1158101	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1159624	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11733262	0.84[ASN][1000 genomes]
rs11935001	0.82[ASN][1000 genomes]
rs11939341	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12504448	0.81[ASN][1000 genomes]
rs12510629	0.81[ASN][1000 genomes]
rs12510870	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13103378	0.81[ASN][1000 genomes]
rs13107306	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13120998	0.81[ASN][1000 genomes]
rs13124940	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13150405	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1358592	0.83[ASN][1000 genomes]
rs1590115	0.80[ASN][1000 genomes]
rs1590116	0.80[ASN][1000 genomes]
rs16849461	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16849484	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16849508	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1894293	0.85[ASN][1000 genomes]
rs1919479	0.80[ASN][1000 genomes]
rs1997332	0.81[ASN][1000 genomes]
rs1997333	0.81[ASN][1000 genomes]
rs2071097	0.81[ASN][1000 genomes]
rs2071098	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2141465	0.81[ASN][1000 genomes]
rs2178290	0.81[ASN][1000 genomes]
rs2178292	0.80[ASN][1000 genomes]
rs2204736	0.80[ASN][1000 genomes]
rs34400902	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34468776	0.82[ASN][1000 genomes]
rs35233345	0.82[ASN][1000 genomes]
rs35858007	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35988516	0.82[ASN][1000 genomes]
rs4235119	0.81[ASN][1000 genomes]
rs4267703	0.81[ASN][1000 genomes]
rs4267704	0.81[ASN][1000 genomes]
rs4267705	0.81[ASN][1000 genomes]
rs4438732	0.80[ASN][1000 genomes]
rs4618279	0.80[ASN][1000 genomes]
rs4694173	0.80[ASN][1000 genomes]
rs56011127	0.80[ASN][1000 genomes]
rs56384466	0.80[ASN][1000 genomes]
rs6446937	0.81[ASN][1000 genomes]
rs6446938	0.81[ASN][1000 genomes]
rs6446939	0.83[ASN][1000 genomes]
rs6852149	0.81[ASN][1000 genomes]
rs6852772	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72647083	0.80[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3430875	chr4:74243646-74420354	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74346000-74348600	Enhancers	HepG2	liver
2	chr4:74346600-74348000	Weak transcription	Pancreas	Pancrea
3	chr4:74346800-74348000	Weak transcription	Fetal Intestine Small	intestine
4	chr4:74347200-74350400	Active TSS	Liver	Liver
5	chr4:74347600-74348400	Enhancers	Fetal Intestine Large	intestine

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