Variant report

Variant	rs7826524
Chromosome Location	chr8:119996675-119996676
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10505350	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10505352	0.83[ASN][1000 genomes]
rs10955918	0.83[ASN][1000 genomes]
rs10955920	0.83[ASN][1000 genomes]
rs10955921	0.83[ASN][1000 genomes]
rs11985044	0.99[ASN][1000 genomes]
rs11986345	0.99[ASN][1000 genomes]
rs11987514	0.94[ASN][1000 genomes]
rs11987528	0.94[ASN][1000 genomes]
rs11990877	0.99[ASN][1000 genomes]
rs11992072	0.98[ASN][1000 genomes]
rs11992370	0.99[ASN][1000 genomes]
rs11994357	0.99[ASN][1000 genomes]
rs12056401	0.80[ASN][1000 genomes]
rs12056490	0.83[ASN][1000 genomes]
rs12056749	0.80[ASN][1000 genomes]
rs12675217	0.88[ASN][1000 genomes]
rs12676636	0.94[ASN][1000 genomes]
rs12677367	0.83[ASN][1000 genomes]
rs12677975	0.88[ASN][1000 genomes]
rs12678216	0.80[ASN][1000 genomes]
rs12679567	0.83[ASN][1000 genomes]
rs12681528	0.83[ASN][1000 genomes]
rs1385507	0.80[ASN][1000 genomes]
rs1385508	0.80[ASN][1000 genomes]
rs1485311	0.80[ASN][1000 genomes]
rs16891854	0.83[ASN][1000 genomes]
rs16891856	0.83[ASN][1000 genomes]
rs16891859	0.83[ASN][1000 genomes]
rs16891861	0.83[ASN][1000 genomes]
rs16891864	0.83[ASN][1000 genomes]
rs16891869	0.83[ASN][1000 genomes]
rs16891872	0.83[ASN][1000 genomes]
rs16891875	0.83[ASN][1000 genomes]
rs16891907	0.80[ASN][1000 genomes]
rs16891911	0.80[ASN][1000 genomes]
rs16891913	0.80[ASN][1000 genomes]
rs16891914	0.80[ASN][1000 genomes]
rs16891916	0.80[ASN][1000 genomes]
rs17758108	0.94[ASN][1000 genomes]
rs17758126	0.94[ASN][1000 genomes]
rs17758162	0.94[ASN][1000 genomes]
rs17758186	0.99[ASN][1000 genomes]
rs17758222	0.96[ASN][1000 genomes]
rs17758258	0.89[ASN][1000 genomes]
rs17758330	0.86[ASN][1000 genomes]
rs17831135	0.94[ASN][1000 genomes]
rs17831147	0.94[ASN][1000 genomes]
rs17831171	0.94[ASN][1000 genomes]
rs17831322	0.89[ASN][1000 genomes]
rs3924060	0.85[ASN][1000 genomes]
rs4437685	0.83[ASN][1000 genomes]
rs4565488	0.83[ASN][1000 genomes]
rs56764969	0.94[ASN][1000 genomes]
rs56862071	0.83[ASN][1000 genomes]
rs58732819	0.83[ASN][1000 genomes]
rs59027630	0.91[ASN][1000 genomes]
rs59943296	0.83[ASN][1000 genomes]
rs60012832	0.83[ASN][1000 genomes]
rs60335297	0.80[ASN][1000 genomes]
rs60360696	0.83[ASN][1000 genomes]
rs60727179	0.83[ASN][1000 genomes]
rs61280141	0.88[ASN][1000 genomes]
rs61364754	0.83[ASN][1000 genomes]
rs61679139	0.83[ASN][1000 genomes]
rs61706918	0.83[ASN][1000 genomes]
rs6469791	0.96[ASN][1000 genomes]
rs6996974	0.99[ASN][1000 genomes]
rs73709519	0.92[ASN][1000 genomes]
rs73709526	0.83[ASN][1000 genomes]
rs73711408	0.94[ASN][1000 genomes]
rs73711412	0.94[ASN][1000 genomes]
rs7823809	0.87[ASN][1000 genomes]
rs7829123	0.94[ASN][1000 genomes]
rs7835846	0.94[ASN][1000 genomes]
rs7837123	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs923100	0.85[ASN][1000 genomes]
rs9642843	0.94[ASN][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	nsv868916	chr8:119911943-120762250	Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	esv2758169	chr8:119943309-120275750	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	esv2759639	chr8:119943309-120275750	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv522241	chr8:119995697-120027871	Weak transcription Enhancers	TF binding region CpG island	2 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	chr8:119992800-120000600	Weak transcription	NHDF-Ad	bronchial
2	chr8:119995400-120001600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links