Variant report

Variant	rs71529112
Chromosome Location	chr8:64970676-64970677
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs13253000	0.94[ASN][1000 genomes]
rs13262233	0.94[ASN][1000 genomes]
rs13270019	0.90[ASN][1000 genomes]
rs13270477	1.00[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs16930838	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2166124	0.91[ASN][1000 genomes]
rs35447159	0.94[ASN][1000 genomes]
rs35601340	0.85[ASN][1000 genomes]
rs35960014	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4147345	0.89[ASN][1000 genomes]
rs58430911	0.90[ASN][1000 genomes]
rs6987804	0.90[ASN][1000 genomes]
rs71529114	0.94[ASN][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	nsv948343	chr8:64804219-65328394	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv890969	chr8:64807144-65047353	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:64969800-64973200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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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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