Variant report

Variant	rs72663217
Chromosome Location	chr8:60941835-60941836
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10957118	0.85[AMR][1000 genomes]
rs6986354	1.00[AFR][1000 genomes]
rs72659758	1.00[AFR][1000 genomes]
rs72661442	0.85[AMR][1000 genomes]
rs72661445	0.85[AMR][1000 genomes]
rs72661495	0.85[AMR][1000 genomes]
rs72663207	0.85[AMR][1000 genomes]
rs72663214	0.85[AMR][1000 genomes]
rs72663216	0.85[AMR][1000 genomes]
rs72663221	0.85[AMR][1000 genomes]
rs72663222	0.85[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831331	chr8:60770382-60959633	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr8:60939800-60943000	Weak transcription	Primary B cells from cord blood	blood
2	chr8:60940000-60942400	Weak transcription	Primary B cells from peripheral blood	blood
3	chr8:60940000-60968400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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