Variant report

Variant	rs29518
Chromosome Location	chr7:41218103-41218104
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10227446	0.84[EUR][1000 genomes]
rs10227663	0.84[EUR][1000 genomes]
rs10258940	0.91[EUR][1000 genomes]
rs10274211	0.91[EUR][1000 genomes]
rs13225532	0.82[ASN][1000 genomes]
rs1859693	0.91[EUR][1000 genomes]
rs2108156	0.90[EUR][1000 genomes]
rs2108157	0.91[EUR][1000 genomes]
rs255012	0.82[ASN][1000 genomes]
rs255014	0.82[ASN][1000 genomes]
rs255015	0.82[ASN][1000 genomes]
rs255017	0.82[ASN][1000 genomes]
rs28176	0.91[ASN][1000 genomes]
rs28238	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28314	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28880	0.91[EUR][1000 genomes]
rs29476	0.91[EUR][1000 genomes]
rs29477	0.91[EUR][1000 genomes]
rs29478	0.90[EUR][1000 genomes]
rs29482	0.91[EUR][1000 genomes]
rs29483	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs29484	0.83[ASN][1000 genomes]
rs29485	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs29486	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs29488	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs29489	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs29490	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs29492	0.85[ASN][1000 genomes]
rs29493	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs29494	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs29495	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs29496	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs29497	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs29498	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs29499	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs29500	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs29501	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs29502	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs29504	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs29505	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs29506	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs29508	0.87[ASN][1000 genomes]
rs29509	0.87[ASN][1000 genomes]
rs29511	0.87[ASN][1000 genomes]
rs29512	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs29513	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs29514	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs29515	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs29519	0.91[ASN][1000 genomes]
rs29521	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs29522	0.91[ASN][1000 genomes]
rs29523	0.89[ASN][1000 genomes]
rs29524	0.90[ASN][1000 genomes]
rs29525	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs29526	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs29530	0.87[ASN][1000 genomes]
rs29532	0.87[ASN][1000 genomes]
rs29537	0.84[ASN][1000 genomes]
rs29539	0.84[ASN][1000 genomes]
rs4720399	0.91[EUR][1000 genomes]
rs4724029	0.84[EUR][1000 genomes]
rs6463005	0.84[EUR][1000 genomes]
rs6463006	0.84[EUR][1000 genomes]
rs6463007	0.84[EUR][1000 genomes]
rs6463008	0.90[EUR][1000 genomes]
rs6945901	0.89[EUR][1000 genomes]
rs6946898	0.88[EUR][1000 genomes]
rs6958423	0.88[EUR][1000 genomes]
rs6971196	0.81[EUR][1000 genomes]
rs7384944	0.88[ASN][1000 genomes]
rs7790556	0.88[EUR][1000 genomes]
rs7805795	0.88[EUR][1000 genomes]
rs9632615	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034605	chr7:41096638-41222426	Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv887989	chr7:41125447-41337044	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1028983	chr7:41165668-41635954	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:41189400-41222400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:41215200-41226600	Weak transcription	Aorta	Aorta
3	chr7:41215400-41230400	Weak transcription	Pancreas	Pancrea
4	chr7:41217400-41218600	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr7:41217400-41218800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr7:41218000-41218800	Weak transcription	HUES64 Cell Line	embryonic stem cell

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