Variant report

Variant	rs2362292
Chromosome Location	chr2:234836770-234836771
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:234835606..234837772-chr2:234955390..234957030,2	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1003540	0.83[AFR][1000 genomes]
rs10166942	0.83[AFR][1000 genomes]
rs10170399	0.83[AFR][1000 genomes]
rs10187654	0.81[AFR][1000 genomes]
rs10189040	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10490012	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10929319	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11563060	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs11563063	0.83[AFR][1000 genomes]
rs11563216	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs13418652	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1985366	0.83[AFR][1000 genomes]
rs2108809	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2215173	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2302153	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2362293	0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4233636	0.92[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs4663983	0.83[AFR][1000 genomes]
rs4663986	0.92[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs4663988	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4663990	0.82[AMR][1000 genomes]
rs6431648	0.92[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs6711120	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6712893	0.81[AMR][1000 genomes]
rs6738375	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6740118	0.82[AMR][1000 genomes]
rs737636	0.90[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs758275	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs758276	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7597012	0.82[AMR][1000 genomes]
rs7604471	0.92[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs917435	0.81[AMR][1000 genomes]
rs9646719	0.81[EUR][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	nsv1013712	chr2:234558457-235495825	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv532476	chr2:234595695-235134381	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234834400-234838000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:234834800-234837200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr2:234836200-234838000	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr2:234836200-234838000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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