Variant report

Variant	rs4669169
Chromosome Location	chr2:7383538-7383539
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:7378951..7380518-chr2:7382090..7384439,2	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs1016515	0.83[ASN][1000 genomes]
rs10929471	0.97[ASN][1000 genomes]
rs10929472	0.93[ASN][1000 genomes]
rs10929473	0.95[ASN][1000 genomes]
rs10929474	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11682417	0.97[ASN][1000 genomes]
rs11687207	0.90[ASN][1000 genomes]
rs11695715	0.81[ASN][1000 genomes]
rs12612059	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12612703	0.81[ASN][1000 genomes]
rs12619070	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12621585	0.81[ASN][1000 genomes]
rs12623613	0.81[ASN][1000 genomes]
rs12999068	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13013964	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13023691	0.81[ASN][1000 genomes]
rs1404845	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1464880	0.92[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs1473655	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1473656	0.80[ASN][1000 genomes]
rs1525490	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1525492	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16866007	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16866008	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16866010	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1880605	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1917678	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2352713	0.83[ASN][1000 genomes]
rs34130652	0.84[ASN][1000 genomes]
rs34325684	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4233854	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4265983	0.90[ASN][1000 genomes]
rs4668527	0.81[ASN][1000 genomes]
rs4668531	0.97[ASN][1000 genomes]
rs4669153	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4669156	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4669158	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4669164	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs55869666	0.92[ASN][1000 genomes]
rs6738582	0.85[ASN][1000 genomes]
rs6739202	0.83[ASN][1000 genomes]
rs7559257	0.94[CEU][hapmap];0.86[CHB][hapmap];0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs872442	0.90[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	nsv915888	chr2:7197783-7461967	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv833337	chr2:7337273-7521146	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:7372000-7388400	Weak transcription	Pancreas	Pancrea
2	chr2:7378000-7388400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:7381600-7387000	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr2:7381800-7383800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr2:7382600-7385600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr2:7382800-7384200	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr2:7383000-7383800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr2:7383200-7399800	Weak transcription	Spleen	Spleen

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