Variant report

Variant	rs35245526
Chromosome Location	chr7:68988182-68988183
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10256483	0.88[EUR][1000 genomes]
rs10257731	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10265122	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10281633	0.86[EUR][1000 genomes]
rs10950189	0.83[EUR][1000 genomes]
rs10950190	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11771876	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12155091	0.85[EUR][1000 genomes]
rs12530810	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12531644	0.94[EUR][1000 genomes]
rs12538348	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12698802	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12698803	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12698804	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13243683	0.85[EUR][1000 genomes]
rs13246613	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1541427	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17137493	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1981585	0.85[EUR][1000 genomes]
rs1981586	0.85[EUR][1000 genomes]
rs2108046	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2865169	0.86[EUR][1000 genomes]
rs28758447	0.88[EUR][1000 genomes]
rs41862	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs41863	0.80[EUR][1000 genomes]
rs41865	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4268006	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs55714924	0.84[EUR][1000 genomes]
rs56854903	0.85[EUR][1000 genomes]
rs6460521	0.86[EUR][1000 genomes]
rs6944163	0.85[EUR][1000 genomes]
rs6946622	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6975413	0.86[EUR][1000 genomes]
rs6979168	0.85[EUR][1000 genomes]
rs73437648	0.89[EUR][1000 genomes]
rs7785268	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7810187	0.85[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	nsv1023885	chr7:68894896-69158290	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv538915	chr7:68894896-69158290	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv916011	chr7:68942155-69330800	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv5782	chr7:68946883-68991904	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 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	chr7:68984000-68991400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:68984000-68999200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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