Variant report

Variant	rs62167935
Chromosome Location	chr2:142280373-142280374
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10496881	0.85[ASN][1000 genomes]
rs11887304	0.85[ASN][1000 genomes]
rs16846183	0.85[ASN][1000 genomes]
rs16846216	0.85[ASN][1000 genomes]
rs16846224	0.85[ASN][1000 genomes]
rs16846251	0.85[ASN][1000 genomes]
rs16846272	0.85[ASN][1000 genomes]
rs16846274	0.85[ASN][1000 genomes]
rs16846416	0.82[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs16846509	0.88[ASN][1000 genomes]
rs16855055	0.94[ASN][1000 genomes]
rs41396347	0.85[ASN][1000 genomes]
rs4271711	0.88[ASN][1000 genomes]
rs4491668	0.85[ASN][1000 genomes]
rs4547471	0.85[ASN][1000 genomes]
rs62167901	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62167934	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72849629	0.85[ASN][1000 genomes]
rs72849660	0.85[ASN][1000 genomes]
rs72849666	0.85[ASN][1000 genomes]
rs72851323	0.85[ASN][1000 genomes]
rs72851325	0.85[ASN][1000 genomes]
rs72851386	0.94[ASN][1000 genomes]
rs72852436	0.94[ASN][1000 genomes]
rs72852464	0.94[ASN][1000 genomes]
rs72853562	0.94[ASN][1000 genomes]
rs72853582	0.94[ASN][1000 genomes]
rs72853591	0.88[ASN][1000 genomes]
rs72853599	0.88[ASN][1000 genomes]
rs72855461	0.83[ASN][1000 genomes]
rs7557886	0.85[ASN][1000 genomes]
rs7576810	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9287319	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817518	chr2:141714174-142287302	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv583203	chr2:142055133-142378975	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv875240	chr2:142199421-142347455	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
4	nsv470491	chr2:142254119-142299923	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
5	nsv834393	chr2:142256714-142431564	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	n/a
6	nsv583210	chr2:142259592-142295042	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
7	nsv459629	chr2:142263400-142295042	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
8	nsv583211	chr2:142263400-142295042	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
9	nsv583212	chr2:142263979-142309330	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:142278200-142280600	Enhancers	Brain Substantia Nigra	brain
2	chr2:142278800-142291200	Weak transcription	Brain Anterior Caudate	brain
3	chr2:142279600-142280600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr2:142279600-142280600	Enhancers	Brain Cingulate Gyrus	brain
5	chr2:142279800-142280800	Bivalent Enhancer	Fetal Heart	heart
6	chr2:142280000-142280600	Enhancers	Brain Angular Gyrus	brain
7	chr2:142280000-142280600	Enhancers	Brain Hippocampus Middle	brain
8	chr2:142280200-142280800	Enhancers	GM12878-XiMat	blood

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