Variant report

Variant	rs7676437
Chromosome Location	chr4:121310333-121310334
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:121309932..121311519-chr4:121313046..121315204,2	K562	blood:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10014014	0.87[EUR][1000 genomes]
rs11098562	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1160185	0.82[EUR][1000 genomes]
rs12374224	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12498541	0.89[ASN][1000 genomes]
rs1448065	0.83[ASN][1000 genomes]
rs1553691	0.87[EUR][1000 genomes]
rs1553692	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17394655	0.89[ASN][1000 genomes]
rs2166838	0.83[EUR][1000 genomes]
rs2662701	0.89[ASN][1000 genomes]
rs2693767	0.87[EUR][1000 genomes]
rs4834842	0.89[ASN][1000 genomes]
rs4834843	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4834844	0.89[ASN][1000 genomes]
rs62322873	0.89[ASN][1000 genomes]
rs62322903	0.97[ASN][1000 genomes]
rs7662231	0.83[ASN][1000 genomes]
rs7666940	0.81[ASN][1000 genomes]
rs7676949	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7698730	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9307486	0.87[EUR][1000 genomes]
rs950657	0.82[EUR][1000 genomes]
rs970429	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007641	chr4:120884220-121555889	Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv537234	chr4:120884220-121555889	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv595333	chr4:121093248-121440368	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1005240	chr4:121093285-121420997	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv879852	chr4:121108734-121768496	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv879853	chr4:121292665-121513215	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:121310200-121310400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links