Variant report

Variant	rs7844749
Chromosome Location	chr8:63510996-63510997
allele	A/T
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:31)

rs_ID	r²[population]
rs12549995	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1351365	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1451856	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1531657	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16929287	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs16929302	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2127577	1.00[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2620876	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2957797	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4483149	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4738986	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4738991	0.83[EUR][1000 genomes]
rs55651027	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs58103443	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs58261377	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62509503	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62509504	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62509505	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6985441	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7812978	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7840692	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs827683	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs827684	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs827687	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs862386	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs936614	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs936616	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs936618	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs936619	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs936620	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs961829	0.87[EUR][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	nsv1018879	chr8:63281724-63937632	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv890959	chr8:63449156-63515522	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	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	chr8:63510600-63512400	Enhancers	Primary B cells from peripheral blood	blood

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