Variant report

Variant	rs7668905
Chromosome Location	chr4:18511568-18511569
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:18503934..18506814-chr4:18510910..18512578,2	MCF-7	breast:
2	chr4:18507185..18508691-chr4:18511489..18513149,2	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs12507937	0.81[EUR][1000 genomes]
rs12507985	0.89[EUR][1000 genomes]
rs12645896	0.88[EUR][1000 genomes]
rs12646058	0.89[ASN][1000 genomes]
rs12646743	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12648980	0.88[EUR][1000 genomes]
rs16897040	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs16897142	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16897144	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2616459	0.89[ASN][1000 genomes]
rs2616460	0.89[ASN][1000 genomes]
rs4521343	0.88[EUR][1000 genomes]
rs56708160	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs66763016	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs67249909	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs67551652	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs67996028	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6812499	0.88[EUR][1000 genomes]
rs6828694	0.89[EUR][1000 genomes]
rs6838041	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6851547	0.86[ASN][1000 genomes]
rs6851929	0.86[ASN][1000 genomes]
rs73232257	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73248757	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73248762	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73248783	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73250405	0.89[EUR][1000 genomes]
rs73250408	0.89[EUR][1000 genomes]
rs7671449	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7673673	0.83[ASN][1000 genomes]
rs7674800	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7684376	0.82[EUR][1000 genomes]
rs906080	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003931	chr4:18241575-18849898	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv533087	chr4:18362040-19176896	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:18509000-18515200	Weak transcription	Fetal Intestine Small	intestine
2	chr4:18510800-18514400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr4:18511200-18513400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr4:18511400-18513400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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