Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs13316480	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs16842308	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs28718846	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4429672	1.00[ASN][1000 genomes]
rs58195225	0.91[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61413999	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62270312	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62270314	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62270315	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62270317	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62270318	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62270321	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs62270322	1.00[ASN][1000 genomes]
rs62273061	1.00[ASN][1000 genomes]
rs66569551	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6764013	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]
rs7636773	1.00[ASN][1000 genomes]
rs983401	1.00[ASN][1000 genomes]
rs9848835	1.00[ASN][1000 genomes]
rs9849294	1.00[ASN][1000 genomes]
rs9859830	1.00[ASN][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:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:134639400-134653800	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr3:134642400-134653800	Weak transcription	Brain Germinal Matrix	brain
3	chr3:134644200-134654800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr3:134644600-134656400	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr3:134649000-134656200	Weak transcription	Fetal Muscle Leg	muscle
6	chr3:134649000-134656200	Weak transcription	Fetal Stomach	stomach
7	chr3:134649200-134652400	Enhancers	Colon Smooth Muscle	Colon
8	chr3:134649800-134653400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr3:134650200-134653200	Weak transcription	Brain Anterior Caudate	brain
10	chr3:134650400-134656000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr3:134650600-134652400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr3:134650600-134652600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr3:134650600-134653600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr3:134650600-134655600	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr3:134650600-134655600	Weak transcription	GM12878-XiMat	blood
16	chr3:134650600-134660600	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr3:134651200-134655800	Weak transcription	Fetal Brain Male	brain
18	chr3:134651400-134653200	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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