Variant report

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs13316480	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16842308	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28718846	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4429672	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58193970	1.00[ASN][1000 genomes]
rs58195225	1.00[ASN][1000 genomes]
rs61413999	1.00[ASN][1000 genomes]
rs62270312	1.00[ASN][1000 genomes]
rs62270314	1.00[ASN][1000 genomes]
rs62270315	1.00[ASN][1000 genomes]
rs62270317	1.00[ASN][1000 genomes]
rs62270318	1.00[ASN][1000 genomes]
rs62270321	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62270322	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62270343	1.00[EUR][1000 genomes]
rs62273061	1.00[ASN][1000 genomes]
rs66868541	0.83[EUR][1000 genomes]
rs6764013	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73214171	1.00[ASN][1000 genomes]
rs73214194	1.00[ASN][1000 genomes]
rs73218226	1.00[ASN][1000 genomes]
rs7614716	1.00[ASN][1000 genomes]
rs7635428	0.97[EUR][1000 genomes]
rs7636773	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs983401	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9848835	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9859830	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9864852	0.83[EUR][1000 genomes]
rs9875045	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:134671000-134684600	Weak transcription	Brain Germinal Matrix	brain
2	chr3:134671000-134693400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
3	chr3:134671000-134697400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr3:134671400-134684400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr3:134673800-134684600	Weak transcription	Brain Cingulate Gyrus	brain
6	chr3:134675200-134684600	Weak transcription	Fetal Brain Female	brain
7	chr3:134677400-134697400	Weak transcription	GM12878-XiMat	blood
8	chr3:134677800-134697000	Weak transcription	Psoas Muscle	Psoas
9	chr3:134678600-134699400	Weak transcription	Aorta	Aorta
10	chr3:134679800-134684400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr3:134680200-134692800	Weak transcription	Spleen	Spleen
12	chr3:134681800-134684200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr3:134682000-134684000	Weak transcription	Fetal Brain Male	brain
14	chr3:134682800-134683000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived

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