Variant report

Variant	rs1579627
Chromosome Location	chr4:96636651-96636652
allele	C/T
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:94)

rs_ID	r²[population]
rs10005387	0.92[ASN][1000 genomes]
rs10006440	0.92[ASN][1000 genomes]
rs10012383	0.93[ASN][1000 genomes]
rs10012443	1.00[ASN][1000 genomes]
rs10024303	0.91[ASN][1000 genomes]
rs10024516	0.90[ASN][1000 genomes]
rs10212842	0.97[ASN][1000 genomes]
rs1025630	0.96[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11097481	0.92[ASN][1000 genomes]
rs1117212	0.93[ASN][1000 genomes]
rs1118569	0.95[ASN][1000 genomes]
rs1118570	0.94[ASN][1000 genomes]
rs12498523	0.92[ASN][1000 genomes]
rs12502426	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12502460	0.92[ASN][1000 genomes]
rs12508146	0.92[ASN][1000 genomes]
rs12640394	0.91[ASN][1000 genomes]
rs12643258	0.91[ASN][1000 genomes]
rs12646632	0.92[ASN][1000 genomes]
rs12649375	0.91[ASN][1000 genomes]
rs12650006	0.88[ASN][1000 genomes]
rs12651480	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs13112111	0.95[ASN][1000 genomes]
rs13112339	0.97[ASN][1000 genomes]
rs13112562	0.97[ASN][1000 genomes]
rs13114915	0.92[ASN][1000 genomes]
rs13122865	0.88[ASN][1000 genomes]
rs13136133	0.95[ASN][1000 genomes]
rs13136911	0.95[ASN][1000 genomes]
rs13139338	0.92[ASN][1000 genomes]
rs13147649	0.92[ASN][1000 genomes]
rs1370002	0.92[ASN][1000 genomes]
rs1370003	0.99[ASN][1000 genomes]
rs1436579	0.95[ASN][1000 genomes]
rs1436583	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1579618	0.92[ASN][1000 genomes]
rs1579619	0.92[ASN][1000 genomes]
rs1579622	0.93[ASN][1000 genomes]
rs1579623	0.93[ASN][1000 genomes]
rs1579626	0.93[ASN][1000 genomes]
rs1595202	0.95[ASN][1000 genomes]
rs1595205	0.92[ASN][1000 genomes]
rs1821738	0.92[ASN][1000 genomes]
rs1821739	0.92[ASN][1000 genomes]
rs1836908	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1865849	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1865850	0.92[ASN][1000 genomes]
rs1865851	0.92[ASN][1000 genomes]
rs1946738	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs1946739	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs1946742	0.80[ASN][1000 genomes]
rs2118052	0.92[ASN][1000 genomes]
rs2164544	0.92[ASN][1000 genomes]
rs2164545	0.92[ASN][1000 genomes]
rs2865468	0.90[ASN][1000 genomes]
rs2865703	0.99[ASN][1000 genomes]
rs2865710	0.91[ASN][1000 genomes]
rs2903012	0.89[ASN][1000 genomes]
rs3975035	0.93[ASN][1000 genomes]
rs4305518	0.90[ASN][1000 genomes]
rs4590043	0.93[ASN][1000 genomes]
rs4699275	0.91[ASN][1000 genomes]
rs4699450	0.92[ASN][1000 genomes]
rs4699451	0.92[ASN][1000 genomes]
rs6821135	0.92[ASN][1000 genomes]
rs6821324	0.91[ASN][1000 genomes]
rs6822198	0.95[ASN][1000 genomes]
rs6833840	0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6843996	0.91[ASN][1000 genomes]
rs6844205	0.91[ASN][1000 genomes]
rs6853495	0.92[ASN][1000 genomes]
rs6854348	0.92[ASN][1000 genomes]
rs7654532	0.90[ASN][1000 genomes]
rs7654785	0.91[ASN][1000 genomes]
rs7655804	0.92[ASN][1000 genomes]
rs7658878	0.92[ASN][1000 genomes]
rs7672473	0.94[ASN][1000 genomes]
rs7680769	0.92[ASN][1000 genomes]
rs7680812	0.92[ASN][1000 genomes]
rs7681281	0.92[ASN][1000 genomes]
rs7691500	0.93[ASN][1000 genomes]
rs7691945	0.93[ASN][1000 genomes]
rs7696585	0.93[ASN][1000 genomes]
rs7698569	0.85[JPT][hapmap];0.84[AMR][1000 genomes]
rs879310	0.97[ASN][1000 genomes]
rs879311	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs879312	0.96[ASN][1000 genomes]
rs893042	0.95[ASN][1000 genomes]
rs9762308	0.95[ASN][1000 genomes]
rs9762310	0.95[ASN][1000 genomes]
rs9993422	0.91[ASN][1000 genomes]
rs9993596	0.92[ASN][1000 genomes]
rs9994206	0.92[ASN][1000 genomes]
rs9994390	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 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	nsv432617	chr4:96627548-96646841	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
9	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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:96636400-96637600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:96636600-96637400	Enhancers	HMEC	breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links