Variant report

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

rs_ID	r²[population]
rs10084416	0.93[ASN][1000 genomes]
rs10490267	0.80[EUR][1000 genomes]
rs10932063	0.95[ASN][1000 genomes]
rs1156249	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11690070	0.95[ASN][1000 genomes]
rs12472876	1.00[ASN][1000 genomes]
rs12616166	0.87[ASN][1000 genomes]
rs13010221	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13024043	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1374708	0.95[ASN][1000 genomes]
rs1374709	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1447488	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1447490	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1447495	0.89[ASN][1000 genomes]
rs17637637	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34157021	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34368384	0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35071164	0.95[EUR][1000 genomes]
rs4675457	0.86[ASN][1000 genomes]
rs71427747	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7602656	0.89[ASN][1000 genomes]
rs959032	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs959033	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	nsv964353	chr2:205303005-205473935	Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv34706	chr2:205309211-205348724	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr2:205312800-205314600	Enhancers	Rectal Smooth Muscle	rectum
2	chr2:205313600-205316600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:205313600-205316800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:205313800-205316000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:205313800-205317000	Enhancers	Colon Smooth Muscle	Colon
6	chr2:205314000-205320000	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr2:205314200-205316600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr2:205314200-205316800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

Quick Search: