Variant report

Variant	rs879311
Chromosome Location	chr4:96653362-96653363
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 103 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:95)

rs_ID	r²[population]
rs10005387	0.86[ASN][1000 genomes]
rs10006440	0.86[ASN][1000 genomes]
rs10012383	0.87[ASN][1000 genomes]
rs10012443	0.93[ASN][1000 genomes]
rs10024303	0.86[ASN][1000 genomes]
rs10024516	0.85[ASN][1000 genomes]
rs10212842	0.96[ASN][1000 genomes]
rs1025630	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11097481	0.86[ASN][1000 genomes]
rs1117212	0.87[ASN][1000 genomes]
rs1118569	0.90[ASN][1000 genomes]
rs1118570	0.89[ASN][1000 genomes]
rs11934284	0.82[AMR][1000 genomes]
rs12498523	0.86[ASN][1000 genomes]
rs12502426	0.96[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs12502460	0.86[ASN][1000 genomes]
rs12508146	0.86[ASN][1000 genomes]
rs12640394	0.85[ASN][1000 genomes]
rs12643258	0.85[ASN][1000 genomes]
rs12646632	0.86[ASN][1000 genomes]
rs12649375	0.85[ASN][1000 genomes]
rs12650006	0.90[ASN][1000 genomes]
rs12651480	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13112111	0.90[ASN][1000 genomes]
rs13112339	0.92[ASN][1000 genomes]
rs13112562	0.92[ASN][1000 genomes]
rs13114915	0.86[ASN][1000 genomes]
rs13122865	0.91[ASN][1000 genomes]
rs13136133	0.90[ASN][1000 genomes]
rs13136911	0.90[ASN][1000 genomes]
rs13139338	0.86[ASN][1000 genomes]
rs13147649	0.86[ASN][1000 genomes]
rs1370002	0.86[ASN][1000 genomes]
rs1370003	0.93[ASN][1000 genomes]
rs1436579	0.90[ASN][1000 genomes]
rs1436583	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1579618	0.86[ASN][1000 genomes]
rs1579619	0.86[ASN][1000 genomes]
rs1579622	0.87[ASN][1000 genomes]
rs1579623	0.87[ASN][1000 genomes]
rs1579626	0.87[ASN][1000 genomes]
rs1579627	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1595202	0.90[ASN][1000 genomes]
rs1595205	0.86[ASN][1000 genomes]
rs1821738	0.86[ASN][1000 genomes]
rs1821739	0.86[ASN][1000 genomes]
rs1836908	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1865849	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1865850	0.86[ASN][1000 genomes]
rs1865851	0.86[ASN][1000 genomes]
rs1946738	0.83[AMR][1000 genomes]
rs1946739	0.83[AMR][1000 genomes]
rs2118052	0.86[ASN][1000 genomes]
rs2164544	0.86[ASN][1000 genomes]
rs2164545	0.86[ASN][1000 genomes]
rs2865468	0.89[ASN][1000 genomes]
rs2865703	0.94[ASN][1000 genomes]
rs2865710	0.84[ASN][1000 genomes]
rs2903012	0.89[ASN][1000 genomes]
rs3975035	0.87[ASN][1000 genomes]
rs4305518	0.89[ASN][1000 genomes]
rs4590043	0.87[ASN][1000 genomes]
rs4699275	0.87[ASN][1000 genomes]
rs4699450	0.86[ASN][1000 genomes]
rs4699451	0.86[ASN][1000 genomes]
rs6821135	0.86[ASN][1000 genomes]
rs6821324	0.85[ASN][1000 genomes]
rs6822198	0.90[ASN][1000 genomes]
rs6833840	0.86[CHB][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.83[AMR][1000 genomes]
rs6843996	0.85[ASN][1000 genomes]
rs6844205	0.85[ASN][1000 genomes]
rs6853495	0.86[ASN][1000 genomes]
rs6854348	0.86[ASN][1000 genomes]
rs7654532	0.84[ASN][1000 genomes]
rs7654785	0.87[ASN][1000 genomes]
rs7655804	0.87[ASN][1000 genomes]
rs7658878	0.86[ASN][1000 genomes]
rs7672473	0.89[ASN][1000 genomes]
rs7680769	0.86[ASN][1000 genomes]
rs7680812	0.86[ASN][1000 genomes]
rs7681281	0.86[ASN][1000 genomes]
rs7691500	0.88[ASN][1000 genomes]
rs7691945	0.88[ASN][1000 genomes]
rs7696585	0.88[ASN][1000 genomes]
rs7698569	0.81[JPT][hapmap];0.83[AMR][1000 genomes]
rs879309	0.81[AFR][1000 genomes]
rs879310	0.96[ASN][1000 genomes]
rs879312	0.96[ASN][1000 genomes]
rs893042	0.99[ASN][1000 genomes]
rs9762308	0.90[ASN][1000 genomes]
rs9762310	0.90[ASN][1000 genomes]
rs9993422	0.85[ASN][1000 genomes]
rs9993596	0.86[ASN][1000 genomes]
rs9994206	0.86[ASN][1000 genomes]
rs9994390	0.86[ASN][1000 genomes]

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	nsv830012	chr4:96547783-96746163	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv1844506	chr4:96554889-96704333	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv997304	chr4:96575198-96861349	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	esv1846406	chr4:96599084-96664321	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1010830	chr4:96607025-96862878	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv537191	chr4:96607025-96862878	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	esv1843331	chr4:96619599-96664321	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
8	nsv594915	chr4:96628653-97086618	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 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	chr4:96649600-96653400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:96651800-96660600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr4:96653200-96653600	Enhancers	HMEC	breast

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