Variant report

Variant	rs167991
Chromosome Location	chr4:173271546-173271547
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11132935	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs11726268	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12502211	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs12509779	0.91[JPT][hapmap]
rs12511688	0.85[CHB][hapmap];0.90[JPT][hapmap]
rs13101363	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13434538	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1484019	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs1552247	0.90[CHB][hapmap];0.95[JPT][hapmap]
rs17288825	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs17288971	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs17289279	0.87[CHB][hapmap];0.95[JPT][hapmap]
rs2332481	0.96[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2626608	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs2930204	0.86[CHB][hapmap];0.95[JPT][hapmap]
rs333398	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs333399	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs333408	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34069532	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4692917	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6553625	0.96[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap]
rs6836161	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs768425	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs975588	0.85[CHB][hapmap];0.95[JPT][hapmap]

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	nsv1031592	chr4:173112542-173662991	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv537359	chr4:173112542-173662991	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv534293	chr4:173121379-173606082	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:173270000-173276800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:173270400-173273800	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr4:173270800-173273400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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