Variant report

Variant	rs10503698
Chromosome Location	chr8:20979708-20979709
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10111769	0.82[ASN][1000 genomes]
rs10112502	0.96[ASN][1000 genomes]
rs11990863	0.84[ASN][1000 genomes]
rs11996651	0.86[ASN][1000 genomes]
rs12674821	0.85[ASN][1000 genomes]
rs12675109	0.86[ASN][1000 genomes]
rs12676979	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12677314	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12678981	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs12679819	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12679855	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12680270	0.86[ASN][1000 genomes]
rs12680287	0.87[ASN][1000 genomes]
rs12681224	0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1563919	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1563920	0.86[ASN][1000 genomes]
rs1563921	0.86[ASN][1000 genomes]
rs17605964	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1841510	0.95[ASN][1000 genomes]
rs2631894	0.85[ASN][1000 genomes]
rs34133224	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34326138	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34402513	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs35089394	0.86[ASN][1000 genomes]
rs35393501	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35508548	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35923081	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3903353	0.91[ASN][1000 genomes]
rs4739209	0.86[ASN][1000 genomes]
rs4739280	0.83[ASN][1000 genomes]
rs57399105	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs60715093	0.85[AMR][1000 genomes]
rs7015657	0.88[ASN][1000 genomes]
rs898648	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032450	chr8:20514995-21033577	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv539524	chr8:20514995-21033577	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv1034265	chr8:20742935-21152545	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv539528	chr8:20742935-21152545	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv831260	chr8:20907266-21097125	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv469878	chr8:20955260-21128307	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv482339	chr8:20955260-21128307	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:20977600-20983000	Weak transcription	Fetal Muscle Leg	muscle

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