Variant report

Variant	rs13353732
Chromosome Location	chr4:74397154-74397155
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AFM-1	chr4:74396768-74398790	XLOC_003572

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs10004505	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10016403	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10019146	0.88[CEU][hapmap]
rs10028196	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10028276	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10029673	0.87[CEU][hapmap]
rs10212657	0.85[EUR][1000 genomes]
rs10213305	0.85[EUR][1000 genomes]
rs10518115	1.00[CHB][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs10805065	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10938077	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10938078	0.84[CEU][hapmap];0.87[YRI][hapmap];0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10938079	0.84[CEU][hapmap];0.83[YRI][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10938085	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10938086	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1159624	0.81[EUR][1000 genomes]
rs11728915	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11733262	0.83[YRI][hapmap];0.85[EUR][1000 genomes]
rs11935001	0.85[EUR][1000 genomes]
rs11939341	0.83[EUR][1000 genomes]
rs11943798	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1247668	0.89[CEU][hapmap]
rs12503916	0.88[CEU][hapmap]
rs12504448	0.92[EUR][1000 genomes]
rs12507775	0.88[CEU][hapmap]
rs12508974	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12510629	0.87[EUR][1000 genomes]
rs12510870	0.83[CHB][hapmap];0.94[JPT][hapmap]
rs13103378	0.87[EUR][1000 genomes]
rs13115877	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13120998	0.87[EUR][1000 genomes]
rs13124940	0.81[YRI][hapmap];0.83[EUR][1000 genomes]
rs13144296	0.88[CEU][hapmap]
rs1528917	0.89[CEU][hapmap]
rs1528918	0.86[CEU][hapmap]
rs1528924	0.87[EUR][1000 genomes]
rs1569204	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1590115	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1590116	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16849628	0.88[CEU][hapmap]
rs16849677	0.89[CEU][hapmap]
rs16849727	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1881611	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1894293	0.85[EUR][1000 genomes]
rs1919469	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1919479	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1997332	0.84[CEU][hapmap];0.88[YRI][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1997333	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2008288	0.89[CEU][hapmap]
rs2040354	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2071097	0.92[EUR][1000 genomes]
rs2141465	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2141470	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2178290	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2178292	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28838047	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34238679	0.86[EUR][1000 genomes]
rs34468776	0.85[EUR][1000 genomes]
rs35233345	0.85[EUR][1000 genomes]
rs3756073	0.90[ASN][1000 genomes]
rs4235119	0.89[CEU][hapmap];0.84[YRI][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4267703	0.85[CEU][hapmap];0.88[YRI][hapmap];0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4267704	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4267705	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4438732	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4574378	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4618279	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4694170	1.00[CHB][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs4694173	0.87[EUR][1000 genomes]
rs56011127	0.87[EUR][1000 genomes]
rs56384466	0.87[EUR][1000 genomes]
rs6446937	0.86[YRI][hapmap];0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6446938	0.84[CEU][hapmap];0.87[YRI][hapmap];0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6446939	0.89[EUR][1000 genomes]
rs6446941	0.87[EUR][1000 genomes]
rs6837506	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6838329	0.87[ASN][1000 genomes]
rs6852149	0.85[CEU][hapmap];0.92[EUR][1000 genomes]
rs72647083	0.86[EUR][1000 genomes]
rs72649103	0.87[ASN][1000 genomes]
rs7676460	0.81[EUR][1000 genomes]
rs7682201	0.88[CEU][hapmap]
rs7687216	0.90[ASN][1000 genomes]
rs9990707	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9997572	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9999939	0.89[CEU][hapmap]

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	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
2	nsv1001725	chr4:74354050-74860924	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv530126	chr4:74376622-74843892	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	esv3364178	chr4:74383966-74400177	Enhancers Bivalent Enhancer Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers	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	chr4:74374600-74399000	Weak transcription	Fetal Intestine Large	intestine
2	chr4:74390400-74399800	Weak transcription	Fetal Intestine Small	intestine
3	chr4:74394200-74400000	Genic enhancers	Liver	Liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links