Variant report

Variant	rs2292659
Chromosome Location	chr3:134567454-134567455
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:134562864..134564396-chr3:134566053..134568096,2	K562	blood:
2	chr3:134550436..134552836-chr3:134565260..134567786,2	K562	blood:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11928990	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12496060	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13073658	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13079457	0.89[CHB][hapmap]
rs13090529	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13090749	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13090758	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13091440	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1949305	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2292660	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2895697	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34894066	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35520698	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35600864	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35988574	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3732569	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6439529	0.89[CHB][hapmap]
rs6762261	0.89[CHB][hapmap];0.84[YRI][hapmap]
rs6782516	0.89[CHB][hapmap]
rs6797336	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6801877	1.00[CEU][hapmap];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72984008	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7634094	0.83[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.83[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	nsv877515	chr3:134460368-134591138	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1009634	chr3:134543259-134820208	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv536720	chr3:134543259-134820208	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1000277	chr3:134546080-134970837	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:134549800-134569400	Weak transcription	Fetal Brain Male	brain
2	chr3:134564600-134568200	Weak transcription	GM12878-XiMat	blood
3	chr3:134564600-134568600	Weak transcription	Psoas Muscle	Psoas
4	chr3:134565600-134569600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr3:134566000-134569600	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr3:134566200-134569200	Weak transcription	Fetal Muscle Trunk	muscle
7	chr3:134566200-134569400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr3:134566400-134568400	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr3:134566600-134567800	Weak transcription	Spleen	Spleen
10	chr3:134566600-134568200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr3:134566600-134568600	Weak transcription	Fetal Muscle Leg	muscle
12	chr3:134566600-134569000	Weak transcription	Adipose Nuclei	Adipose
13	chr3:134566600-134569200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr3:134566600-134569200	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr3:134566800-134567800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr3:134566800-134569400	Weak transcription	Left Ventricle	heart
17	chr3:134566800-134569800	Weak transcription	Duodenum Mucosa	Duodenum
18	chr3:134567200-134569600	Weak transcription	HUVEC	blood vessel
19	chr3:134567200-134576000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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