Variant report

Variant	rs4489344
Chromosome Location	chr8:49133980-49133981
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10099462	0.90[EUR][1000 genomes]
rs10429272	0.87[CHB][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10808911	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10958494	0.89[YRI][hapmap]
rs11778279	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11783647	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11783734	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12675189	0.87[CHB][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34568428	0.82[AFR][1000 genomes]
rs3934732	0.80[AFR][1000 genomes]
rs3934734	0.80[AFR][1000 genomes]
rs4242485	0.82[AFR][1000 genomes]
rs4373544	0.80[AFR][1000 genomes]
rs4455863	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4455864	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4475511	0.80[AFR][1000 genomes]
rs4531079	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4534147	0.88[YRI][hapmap];0.80[AFR][1000 genomes]
rs4537328	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4596682	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs4639551	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4873271	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4873788	0.89[YRI][hapmap]
rs6474074	0.80[AFR][1000 genomes]
rs6994417	0.82[AFR][1000 genomes]
rs7815183	0.88[YRI][hapmap];0.82[AFR][1000 genomes]
rs7838270	0.85[AFR][1000 genomes]
rs7838513	0.81[ASN][1000 genomes]
rs7841194	0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831310	chr8:49080177-49256440	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv1841988	chr8:49093467-49156411	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv831311	chr8:49106160-49290209	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	esv16816	chr8:49118221-49166985	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49133400-49134200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr8:49133600-49134000	Enhancers	NHEK	skin

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