Variant report

Variant	rs7702589
Chromosome Location	chr5:124782843-124782844
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs1554281	1.00[AMR][1000 genomes]
rs55717300	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56707415	1.00[AMR][1000 genomes]
rs56821497	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56835569	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56988571	1.00[AMR][1000 genomes]
rs57118683	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57123863	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57697012	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58308815	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58338793	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58631543	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58917396	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59000628	1.00[AMR][1000 genomes]
rs59380738	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60214755	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61304237	1.00[AMR][1000 genomes]
rs61472360	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6595615	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6866932	0.81[AFR][1000 genomes]
rs6866980	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6868024	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6870489	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6875057	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6875229	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6878929	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6883449	1.00[AMR][1000 genomes]
rs6883628	1.00[AMR][1000 genomes]
rs6884059	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6884354	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6887469	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6890153	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6894842	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73303305	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73303332	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303334	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73303374	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73303384	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303399	1.00[AMR][1000 genomes]
rs73303400	1.00[AMR][1000 genomes]
rs73305305	1.00[AMR][1000 genomes]
rs73305308	1.00[AMR][1000 genomes]
rs73305320	1.00[AMR][1000 genomes]
rs73305337	1.00[AMR][1000 genomes]
rs73305339	1.00[AMR][1000 genomes]
rs73305342	1.00[AMR][1000 genomes]
rs73305344	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73305345	1.00[AMR][1000 genomes]
rs73321471	0.81[AFR][1000 genomes]
rs73321473	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7711951	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7725952	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7729702	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7729817	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7730376	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7730445	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7732317	1.00[AMR][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	nsv1030992	chr5:124708549-125391503	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv537892	chr5:124708549-125391503	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr5:124781800-124783400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr5:124782600-124783400	Enhancers	Muscle Satellite Cultured Cells	--
3	chr5:124782800-124783200	Active TSS	A549	lung
4	chr5:124782800-124783400	Enhancers	NHLF	lung

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