Variant report

Variant	rs335340
Chromosome Location	chr4:62329503-62329504
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs1037671	1.00[TSI][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10517536	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11131326	1.00[EUR][1000 genomes]
rs1350247	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1379166	0.91[AMR][1000 genomes]
rs1379167	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1456867	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1456875	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1456876	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1456877	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1456878	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1497902	1.00[EUR][1000 genomes]
rs1497904	1.00[EUR][1000 genomes]
rs1497917	1.00[TSI][hapmap]
rs1531204	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17090502	1.00[EUR][1000 genomes]
rs17090511	1.00[EUR][1000 genomes]
rs17090512	1.00[EUR][1000 genomes]
rs17090513	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs1845582	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2124795	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2124796	1.00[EUR][1000 genomes]
rs2219342	1.00[EUR][1000 genomes]
rs2606712	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2606714	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2606715	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2606716	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2606717	1.00[TSI][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2606718	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2606720	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2643035	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2643037	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2643038	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2643039	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2643040	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs335274	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs335275	1.00[EUR][1000 genomes]
rs335276	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs335277	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs335278	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs335280	1.00[TSI][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs335281	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs335282	0.91[AMR][1000 genomes]
rs335283	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs335284	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs335293	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs335297	1.00[EUR][1000 genomes]
rs335298	1.00[EUR][1000 genomes]
rs335326	1.00[EUR][1000 genomes]
rs335327	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs335328	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs335330	1.00[EUR][1000 genomes]
rs335331	1.00[EUR][1000 genomes]
rs335333	1.00[EUR][1000 genomes]
rs335339	1.00[ASW][hapmap];1.00[LWK][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs335343	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs335344	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs335345	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs335346	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs335347	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs335348	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4860413	1.00[EUR][1000 genomes]
rs6551630	1.00[EUR][1000 genomes]
rs6814707	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6823672	1.00[EUR][1000 genomes]
rs6834543	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6841033	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs6856328	1.00[TSI][hapmap]
rs7655377	1.00[EUR][1000 genomes]
rs7660777	1.00[EUR][1000 genomes]
rs7683598	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs7687816	1.00[TSI][hapmap];0.91[AMR][1000 genomes]
rs7693587	1.00[EUR][1000 genomes]
rs7693679	1.00[EUR][1000 genomes]
rs7698624	1.00[EUR][1000 genomes]
rs9654273	1.00[EUR][1000 genomes]
rs991586	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs991587	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs991588	1.00[TSI][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]

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	nsv879075	chr4:62124531-62354791	Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv868844	chr4:62241702-62497248	Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv879076	chr4:62251077-62354791	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv2753138	chr4:62271444-62442507	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:62327400-62330000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr4:62327400-62330600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr4:62328200-62333800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr4:62328200-62333800	Weak transcription	Brain Substantia Nigra	brain
5	chr4:62328400-62330000	Enhancers	HMEC	breast
6	chr4:62328600-62330200	Enhancers	NHEK	skin
7	chr4:62328600-62330600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr4:62328800-62333600	Weak transcription	Brain Hippocampus Middle	brain
9	chr4:62329000-62329800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:62329000-62333600	Weak transcription	NH-A	brain
11	chr4:62329200-62333600	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr4:62329400-62335000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links